ENST00000281928.9:c.4959T>C
MANE Select
|
ENSP00000281928.3:p.Val1653=
|
|
ENST00000549786.2:c.4387T>C
|
|
|
ENST00000648379.1:n.3327T>C
|
|
|
ENST00000648737.1:n.4723T>C
|
|
|
ENST00000648825.1:n.1699T>C
|
|
|
ENST00000648916.1:n.2970T>C
|
|
|
ENST00000649146.1:n.2202T>C
|
|
|
ENST00000649607.1:c.3143T>C
|
|
|
ENST00000649775.1:c.1453-5T>C
|
|
|
ENST00000650226.1:c.4959T>C
|
ENSP00000496981.1:p.Val1653=
|
|
ENST00000281928.7:c.4959T>C
|
ENSP00000281928.3:p.Val1653=
|
|
ENST00000549786.1:c.323T>C
|
|
|
NM_015335.4:c.4959T>C
|
NP_056150.1:p.Val1653=
|
|
XM_011538080.1:c.4959T>C
|
XP_011536382.1:p.Val1653=
|
|
XM_011538081.1:c.4956T>C
|
XP_011536383.1:p.Val1652=
|
|
XM_011538082.1:c.4929T>C
|
XP_011536384.1:p.Val1643=
|
|
XM_011538080.2:c.4959T>C
|
XP_011536382.1:p.Val1653=
|
|
XM_011538081.2:c.4956T>C
|
XP_011536383.1:p.Val1652=
|
|
XM_011538082.2:c.4929T>C
|
XP_011536384.1:p.Val1643=
|
|
XM_017019090.1:c.4956T>C
|
XP_016874579.1:p.Val1652=
|
|
NM_015335.5:c.4959T>C
MANE Select
|
NP_056150.1:p.Val1653=
|
|