|
NM_001372.4:c.11406+1G>T
MANE Select
|
NP_001363.2:n.11406+1G>T
|
|
ENST00000262442.9:c.11406+1G>T
MANE Select
|
ENSP00000262442.3:n.11406+1G>T
|
|
NM_001372.3:c.11406+1G>T
|
NP_001363.2:n.11406+1G>T
|
|
NM_004662.2:c.342+1G>T
|
NP_004653.2:n.342+1G>T
|
|
ENST00000262442.8:c.11406+1G>T
|
ENSP00000262442.3:n.11406+1G>T
|
|
ENST00000396001.6:n.869+1G>T
|
|
|
ENST00000454412.6:c.11406+1G>T
|
ENSP00000414874.2:n.11406+1G>T
|
|
ENST00000581682.1:n.687+1G>T
|
|
|
ENST00000608377.5:c.342+1G>T
|
ENSP00000476951.1:n.342+1G>T
|
|
XM_011523703.1:c.11406+1G>T
|
XP_011522005.1:n.11406+1G>T
|
|
XM_011523703.2:c.11406+1G>T
|
XP_011522005.1:n.11406+1G>T
|
|
XM_017024292.2:c.11289+1G>T
|
XP_016879781.1:n.11289+1G>T
|
|
XM_017024293.1:c.9288+1G>T
|
XP_016879782.1:n.9288+1G>T
|