ENST00000281928.9:c.4401G>C
MANE Select
|
ENSP00000281928.3:p.Val1467=
|
|
ENST00000549786.2:c.3829G>C
|
|
|
ENST00000648379.1:n.2769G>C
|
|
|
ENST00000648737.1:n.4165G>C
|
|
|
ENST00000648825.1:n.1141G>C
|
|
|
ENST00000648916.1:n.2412G>C
|
|
|
ENST00000649146.1:n.1131G>C
|
|
|
ENST00000649607.1:c.2585G>C
|
|
|
ENST00000649775.1:c.898G>C
|
|
|
ENST00000650091.1:n.2377G>C
|
|
|
ENST00000650226.1:c.4401G>C
|
ENSP00000496981.1:p.Val1467=
|
|
ENST00000281928.7:c.4401G>C
|
ENSP00000281928.3:p.Val1467=
|
|
NM_015335.4:c.4401G>C
|
NP_056150.1:p.Val1467=
|
|
XM_011538080.1:c.4401G>C
|
XP_011536382.1:p.Val1467=
|
|
XM_011538081.1:c.4398G>C
|
XP_011536383.1:p.Val1466=
|
|
XM_011538082.1:c.4371G>C
|
XP_011536384.1:p.Val1457=
|
|
XM_011538080.2:c.4401G>C
|
XP_011536382.1:p.Val1467=
|
|
XM_011538081.2:c.4398G>C
|
XP_011536383.1:p.Val1466=
|
|
XM_011538082.2:c.4371G>C
|
XP_011536384.1:p.Val1457=
|
|
XM_017019090.1:c.4398G>C
|
XP_016874579.1:p.Val1466=
|
|
NM_015335.5:c.4401G>C
MANE Select
|
NP_056150.1:p.Val1467=
|
|