ENST00000348931.9:c.407-226C>G
MANE Select
|
ENSP00000335384.5:n.407-226C>G
|
|
ENST00000348931.8:c.407-226C>G
|
ENSP00000335384.5:n.407-226C>G
|
|
ENST00000377940.3:c.341-226C>G
|
ENSP00000367174.3:n.341-226C>G
|
|
ENST00000583811.5:c.53-226C>G
|
ENSP00000462463.1:n.53-226C>G
|
|
ENST00000584588.5:c.406+419C>G
|
ENSP00000462067.1:n.406+419C>G
|
|
NM_198844.2:c.341-226C>G
|
NP_942141.2:n.341-226C>G
|
|
NM_199321.2:c.407-226C>G
|
NP_955353.1:n.407-226C>G
|
|
XM_011524298.1:c.407-226C>G
|
XP_011522600.1:n.407-226C>G
|
|
XR_002957959.1:n.598-226C>G
|
|
|
NM_198844.3:c.341-226C>G
|
NP_942141.2:n.341-226C>G
|
|
NM_199321.3:c.407-226C>G
MANE Select
|
NP_955353.1:n.407-226C>G
|
|