ENST00000622290.5:c.*316G>T
|
ENSP00000483331.2:n.*316G>T
|
|
ENST00000205557.12:c.4144G>T
MANE Select
|
ENSP00000205557.7:p.Ala1382Ser
|
|
ENST00000640696.1:c.958G>T
|
ENSP00000492197.1:p.Ala320Ser
|
|
ENST00000205557.11:c.4144G>T
|
ENSP00000205557.7:p.Ala1382Ser
|
|
ENST00000456970.6:c.3769G>T
|
ENSP00000405002.2:n.3769G>T
|
|
ENST00000576204.5:n.1007G>T
|
|
|
ENST00000622290.4:c.*1353G>T
|
ENSP00000483331.1:n.*1353G>T
|
|
NM_001171.5:c.4144G>T
|
NP_001162.4:p.Ala1382Ser
|
|
XM_011522479.1:c.4111G>T
|
XP_011520781.1:p.Ala1371Ser
|
|
XM_011522480.1:c.3802G>T
|
XP_011520782.1:p.Ala1268Ser
|
|
XM_011522481.1:c.3802G>T
|
XP_011520783.1:p.Ala1268Ser
|
|
XR_933134.1:n.539-5089C>A
|
|
|
NM_001351800.1:c.3802G>T
|
NP_001338729.1:p.Ala1268Ser
|
|
NR_147784.1:n.3806G>T
|
|
|
XM_011522479.2:c.4111G>T
|
XP_011520781.1:p.Ala1371Ser
|
|
XM_011522481.3:c.3802G>T
|
XP_011520783.1:p.Ala1268Ser
|
|
XM_017023212.1:c.3976G>T
|
XP_016878701.1:p.Ala1326Ser
|
|
XM_024450261.1:c.4180G>T
|
XP_024306029.1:p.Ala1394Ser
|
|
NM_001171.6:c.4144G>T
MANE Select
|
NP_001162.5:p.Ala1382Ser
|
|