ENST00000281928.9:c.4956-102T>G
MANE Select
|
ENSP00000281928.3:n.4956-102T>G
|
|
ENST00000549786.2:c.4384-102T>G
|
|
|
ENST00000648379.1:n.3324-102T>G
|
|
|
ENST00000648737.1:n.4720-102T>G
|
|
|
ENST00000648825.1:n.1696-102T>G
|
|
|
ENST00000648916.1:n.2967-102T>G
|
|
|
ENST00000649146.1:n.2097T>G
|
|
|
ENST00000649607.1:c.3140-102T>G
|
|
|
ENST00000649775.1:c.1453-110T>G
|
|
|
ENST00000650226.1:c.4956-102T>G
|
ENSP00000496981.1:n.4956-102T>G
|
|
ENST00000281928.7:c.4956-102T>G
|
ENSP00000281928.3:n.4956-102T>G
|
|
ENST00000549786.1:c.320-102T>G
|
|
|
NM_015335.4:c.4956-102T>G
|
NP_056150.1:n.4956-102T>G
|
|
XM_011538080.1:c.4956-102T>G
|
XP_011536382.1:n.4956-102T>G
|
|
XM_011538081.1:c.4953-102T>G
|
XP_011536383.1:n.4953-102T>G
|
|
XM_011538082.1:c.4926-102T>G
|
XP_011536384.1:n.4926-102T>G
|
|
XM_011538080.2:c.4956-102T>G
|
XP_011536382.1:n.4956-102T>G
|
|
XM_011538081.2:c.4953-102T>G
|
XP_011536383.1:n.4953-102T>G
|
|
XM_011538082.2:c.4926-102T>G
|
XP_011536384.1:n.4926-102T>G
|
|
XM_017019090.1:c.4953-102T>G
|
XP_016874579.1:n.4953-102T>G
|
|
NM_015335.5:c.4956-102T>G
MANE Select
|
NP_056150.1:n.4956-102T>G
|
|