ENST00000326735.13:c.3522G>A
MANE Select
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ENSP00000327214.8:p.Leu1174=
|
|
ENST00000326735.12:c.3522G>A
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ENSP00000327214.8:p.Leu1174=
|
|
ENST00000341676.9:c.3220G>A
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ENSP00000341115.5:p.Ala1074Thr
|
|
ENST00000452699.5:c.3507G>A
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ENSP00000413307.1:p.Leu1169=
|
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ENST00000466561.1:n.1568G>A
|
|
|
ENST00000502418.1:c.940G>A
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ENSP00000423065.1:p.Ala314Thr
|
|
NM_001141973.2:c.3507G>A
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NP_001135445.1:p.Leu1169=
|
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NM_001141974.2:c.3220G>A
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NP_001135446.1:p.Ala1074Thr
|
|
NM_022089.3:c.3522G>A
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NP_071372.1:p.Leu1174=
|
|
XM_005245809.1:c.3352G>A
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XP_005245866.1:p.Ala1118Thr
|
|
XM_005245810.1:c.3349G>A
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XP_005245867.1:p.Ala1117Thr
|
|
XM_005245811.1:c.3337G>A
|
XP_005245868.1:p.Ala1113Thr
|
|
XM_005245812.1:c.3325G>A
|
XP_005245869.1:p.Ala1109Thr
|
|
XM_005245813.1:c.3292G>A
|
XP_005245870.1:p.Ala1098Thr
|
|
XM_005245815.1:c.3235G>A
|
XP_005245872.1:p.Ala1079Thr
|
|
XM_006710512.1:c.3334G>A
|
XP_006710575.1:p.Ala1112Thr
|
|
XM_006710513.1:c.3310G>A
|
XP_006710576.1:p.Ala1104Thr
|
|
XM_011541128.1:c.3337G>A
|
XP_011539430.1:p.Ala1113Thr
|
|
XM_011541129.1:c.3145G>A
|
XP_011539431.1:p.Ala1049Thr
|
|
XM_017000844.1:c.3507G>A
|
XP_016856333.1:p.Leu1169=
|
|
XM_017000845.1:c.3504G>A
|
XP_016856334.1:p.Leu1168=
|
|
XM_017000846.1:c.3480G>A
|
XP_016856335.1:p.Leu1160=
|
|
XM_017000847.1:c.3477G>A
|
XP_016856336.1:p.Leu1159=
|
|
XM_017000848.1:c.3405G>A
|
XP_016856337.1:p.Leu1135=
|
|
XM_017000849.1:c.3390G>A
|
XP_016856338.1:p.Leu1130=
|
|
XM_017000850.1:c.3315G>A
|
XP_016856339.1:p.Leu1105=
|
|
NM_022089.4:c.3522G>A
MANE Select
|
NP_071372.1:p.Leu1174=
|
|
NM_001141973.3:c.3507G>A
|
NP_001135445.1:p.Leu1169=
|
|
NM_001141974.3:c.3220G>A
|
NP_001135446.1:p.Ala1074Thr
|
|