ENST00000261937.11:c.4091A>C
MANE Select
|
ENSP00000261937.6:p.Ter1364Ser
|
|
ENST00000261937.10:c.4091A>C
|
ENSP00000261937.6:p.Ter1364Ser
|
|
ENST00000502603.5:n.791A>C
|
|
|
NM_182925.4:c.4091A>C
|
NP_891555.2:p.Ter1364Ser
|
|
XM_011534477.1:c.4340A>C
|
XP_011532779.1:p.Ter1447Ser
|
|
XM_011534478.1:c.4322A>C
|
XP_011532780.1:p.Ter1441Ser
|
|
XM_011534482.1:c.4109A>C
|
XP_011532784.1:p.Ter1370Ser
|
|
XM_011534483.1:c.4031A>C
|
XP_011532785.1:p.Ter1344Ser
|
|
XM_011534484.1:c.3632A>C
|
XP_011532786.1:p.Ter1211Ser
|
|
XR_941095.1:n.4377A>C
|
|
|
XM_011534478.3:c.4322A>C
|
XP_011532780.1:p.Ter1441Ser
|
|
XM_011534484.2:c.3632A>C
|
XP_011532786.1:p.Ter1211Ser
|
|
XM_017009263.1:c.*237A>C
|
XP_016864752.1:n.*237A>C
|
|
XM_017009268.1:c.4013A>C
|
XP_016864757.1:p.Ter1338Ser
|
|
XR_001742050.2:n.4581A>C
|
|
|
NM_182925.5:c.4091A>C
MANE Select
|
NP_891555.2:p.Ter1364Ser
|
|