ENST00000261937.11:c.3895T>A
MANE Select
|
ENSP00000261937.6:p.Cys1299Ser
|
|
ENST00000261937.10:c.3895T>A
|
ENSP00000261937.6:p.Cys1299Ser
|
|
ENST00000502603.5:n.595T>A
|
|
|
NM_182925.4:c.3895T>A
|
NP_891555.2:p.Cys1299Ser
|
|
XM_011534477.1:c.4144T>A
|
XP_011532779.1:p.Cys1382Ser
|
|
XM_011534478.1:c.4126T>A
|
XP_011532780.1:p.Cys1376Ser
|
|
XM_011534479.1:c.*41T>A
|
XP_011532781.1:n.*41T>A
|
|
XM_011534482.1:c.3913T>A
|
XP_011532784.1:p.Cys1305Ser
|
|
XM_011534483.1:c.3835T>A
|
XP_011532785.1:p.Cys1279Ser
|
|
XM_011534484.1:c.3436T>A
|
XP_011532786.1:p.Cys1146Ser
|
|
XR_941095.1:n.4181T>A
|
|
|
XM_011534478.3:c.4126T>A
|
XP_011532780.1:p.Cys1376Ser
|
|
XM_011534484.2:c.3436T>A
|
XP_011532786.1:p.Cys1146Ser
|
|
XM_017009263.1:c.*41T>A
|
XP_016864752.1:n.*41T>A
|
|
XM_017009268.1:c.3817T>A
|
XP_016864757.1:p.Cys1273Ser
|
|
XR_001742050.2:n.4385T>A
|
|
|
NM_182925.5:c.3895T>A
MANE Select
|
NP_891555.2:p.Cys1299Ser
|
|