ENST00000326735.13:c.3460G>T
MANE Select
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ENSP00000327214.8:p.Ala1154Ser
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ENST00000326735.12:c.3460G>T
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ENSP00000327214.8:p.Ala1154Ser
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ENST00000341676.9:c.3158G>T
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ENSP00000341115.5:p.Gly1053Val
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ENST00000452699.5:c.3445G>T
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ENSP00000413307.1:p.Ala1149Ser
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ENST00000466561.1:n.1506G>T
|
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ENST00000502418.1:c.878G>T
|
ENSP00000423065.1:p.Gly293Val
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NM_001141973.2:c.3445G>T
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NP_001135445.1:p.Ala1149Ser
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NM_001141974.2:c.3158G>T
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NP_001135446.1:p.Gly1053Val
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NM_022089.3:c.3460G>T
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NP_071372.1:p.Ala1154Ser
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XM_005245809.1:c.3290G>T
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XP_005245866.1:p.Gly1097Val
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XM_005245810.1:c.3287G>T
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XP_005245867.1:p.Gly1096Val
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XM_005245811.1:c.3275G>T
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XP_005245868.1:p.Gly1092Val
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XM_005245812.1:c.3263G>T
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XP_005245869.1:p.Gly1088Val
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XM_005245813.1:c.3230G>T
|
XP_005245870.1:p.Gly1077Val
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XM_005245815.1:c.3173G>T
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XP_005245872.1:p.Gly1058Val
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XM_006710512.1:c.3272G>T
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XP_006710575.1:p.Gly1091Val
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XM_006710513.1:c.3248G>T
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XP_006710576.1:p.Gly1083Val
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XM_011541128.1:c.3275G>T
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XP_011539430.1:p.Gly1092Val
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XM_011541129.1:c.3083G>T
|
XP_011539431.1:p.Gly1028Val
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XM_017000844.1:c.3445G>T
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XP_016856333.1:p.Ala1149Ser
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XM_017000845.1:c.3442G>T
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XP_016856334.1:p.Ala1148Ser
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XM_017000846.1:c.3418G>T
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XP_016856335.1:p.Ala1140Ser
|
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XM_017000847.1:c.3415G>T
|
XP_016856336.1:p.Ala1139Ser
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XM_017000848.1:c.3343G>T
|
XP_016856337.1:p.Ala1115Ser
|
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XM_017000849.1:c.3328G>T
|
XP_016856338.1:p.Ala1110Ser
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XM_017000850.1:c.3253G>T
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XP_016856339.1:p.Ala1085Ser
|
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NM_022089.4:c.3460G>T
MANE Select
|
NP_071372.1:p.Ala1154Ser
|
|
NM_001141973.3:c.3445G>T
|
NP_001135445.1:p.Ala1149Ser
|
|
NM_001141974.3:c.3158G>T
|
NP_001135446.1:p.Gly1053Val
|
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