ENST00000281928.9:c.3468C>A
MANE Select
|
ENSP00000281928.3:p.Asp1156Glu
|
|
ENST00000549786.2:c.2896C>A
|
|
|
ENST00000648379.1:n.1836C>A
|
|
|
ENST00000648737.1:n.3232C>A
|
|
|
ENST00000648825.1:n.208C>A
|
|
|
ENST00000648916.1:n.1479C>A
|
|
|
ENST00000649607.1:c.1652C>A
|
|
|
ENST00000650226.1:c.3468C>A
|
ENSP00000496981.1:p.Asp1156Glu
|
|
ENST00000281928.7:c.3468C>A
|
ENSP00000281928.3:p.Asp1156Glu
|
|
NM_015335.4:c.3468C>A
|
NP_056150.1:p.Asp1156Glu
|
|
XM_011538080.1:c.3468C>A
|
XP_011536382.1:p.Asp1156Glu
|
|
XM_011538081.1:c.3465C>A
|
XP_011536383.1:p.Asp1155Glu
|
|
XM_011538082.1:c.3438C>A
|
XP_011536384.1:p.Asp1146Glu
|
|
XM_011538080.2:c.3468C>A
|
XP_011536382.1:p.Asp1156Glu
|
|
XM_011538081.2:c.3465C>A
|
XP_011536383.1:p.Asp1155Glu
|
|
XM_011538082.2:c.3438C>A
|
XP_011536384.1:p.Asp1146Glu
|
|
XM_017019090.1:c.3465C>A
|
XP_016874579.1:p.Asp1155Glu
|
|
NM_015335.5:c.3468C>A
MANE Select
|
NP_056150.1:p.Asp1156Glu
|
|