ENST00000642418.1:n.2309C>T
|
|
|
ENST00000643693.1:n.1847C>T
|
|
|
ENST00000644795.1:c.1837C>T
|
ENSP00000495720.1:p.Gln613Ter
|
|
ENST00000646782.1:n.2779C>T
|
|
|
ENST00000647165.2:c.10045C>T
MANE Select
|
ENSP00000495481.1:p.Gln3349Ter
|
|
ENST00000651214.1:n.2476C>T
|
|
|
ENST00000205890.9:c.10045C>T
|
ENSP00000205890.5:p.Gln3349Ter
|
|
ENST00000418233.7:c.1837C>T
|
ENSP00000408800.3:p.Gln613Ter
|
|
ENST00000433411.7:n.1495C>T
|
|
|
ENST00000445289.6:n.814C>T
|
|
|
ENST00000578575.1:c.447C>T
|
|
|
ENST00000579848.6:c.502+3848C>T
|
ENSP00000465910.1:n.502+3848C>T
|
|
ENST00000615845.4:c.10045C>T
|
ENSP00000481642.1:p.Gln3349Ter
|
|
NM_016239.3:c.10045C>T
|
NP_057323.3:p.Gln3349Ter
|
|
XM_011523921.1:c.10039C>T
|
XP_011522223.1:p.Gln3347Ter
|
|
XM_017024714.2:c.9985C>T
|
XP_016880203.1:p.Gln3329Ter
|
|
XM_017024715.2:c.10048C>T
|
XP_016880204.1:p.Gln3350Ter
|
|
NM_016239.4:c.10045C>T
MANE Select
|
NP_057323.3:p.Gln3349Ter
|
|