ENST00000326735.13:c.*69G>A
MANE Select
|
ENSP00000327214.8:n.*69G>A
|
|
ENST00000326735.12:c.*69G>A
|
ENSP00000327214.8:n.*69G>A
|
|
ENST00000341676.9:c.3310G>A
|
ENSP00000341115.5:p.Ala1104Thr
|
|
ENST00000452699.5:c.*69G>A
|
ENSP00000413307.1:n.*69G>A
|
|
ENST00000466561.1:n.1658G>A
|
|
|
ENST00000502418.1:c.1030G>A
|
ENSP00000423065.1:p.Ala344Thr
|
|
NM_001141973.2:c.*69G>A
|
NP_001135445.1:n.*69G>A
|
|
NM_001141974.2:c.3310G>A
|
NP_001135446.1:p.Ala1104Thr
|
|
NM_022089.3:c.*69G>A
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NP_071372.1:n.*69G>A
|
|
XM_005245809.1:c.3442G>A
|
XP_005245866.1:p.Ala1148Thr
|
|
XM_005245810.1:c.3439G>A
|
XP_005245867.1:p.Ala1147Thr
|
|
XM_005245811.1:c.3427G>A
|
XP_005245868.1:p.Ala1143Thr
|
|
XM_005245812.1:c.3415G>A
|
XP_005245869.1:p.Ala1139Thr
|
|
XM_005245813.1:c.3382G>A
|
XP_005245870.1:p.Ala1128Thr
|
|
XM_005245815.1:c.3325G>A
|
XP_005245872.1:p.Ala1109Thr
|
|
XM_006710512.1:c.3424G>A
|
XP_006710575.1:p.Ala1142Thr
|
|
XM_006710513.1:c.3400G>A
|
XP_006710576.1:p.Ala1134Thr
|
|
XM_011541128.1:c.3427G>A
|
XP_011539430.1:p.Ala1143Thr
|
|
XM_011541129.1:c.3235G>A
|
XP_011539431.1:p.Ala1079Thr
|
|
XM_017000844.1:c.*69G>A
|
XP_016856333.1:n.*69G>A
|
|
XM_017000845.1:c.*69G>A
|
XP_016856334.1:n.*69G>A
|
|
XM_017000846.1:c.*69G>A
|
XP_016856335.1:n.*69G>A
|
|
XM_017000847.1:c.*69G>A
|
XP_016856336.1:n.*69G>A
|
|
XM_017000848.1:c.*69G>A
|
XP_016856337.1:n.*69G>A
|
|
XM_017000849.1:c.*69G>A
|
XP_016856338.1:n.*69G>A
|
|
XM_017000850.1:c.*69G>A
|
XP_016856339.1:n.*69G>A
|
|
NM_022089.4:c.*69G>A
MANE Select
|
NP_071372.1:n.*69G>A
|
|
NM_001141973.3:c.*69G>A
|
NP_001135445.1:n.*69G>A
|
|
NM_001141974.3:c.3310G>A
|
NP_001135446.1:p.Ala1104Thr
|
|