ENST00000642418.1:n.1551C>T
|
|
|
ENST00000643693.1:n.1015C>T
|
|
|
ENST00000644795.1:c.1005C>T
|
ENSP00000495720.1:p.Ala335=
|
|
ENST00000646782.1:n.1947C>T
|
|
|
ENST00000647165.2:c.9213C>T
MANE Select
|
ENSP00000495481.1:p.Ala3071=
|
|
ENST00000651214.1:n.1718C>T
|
|
|
ENST00000205890.9:c.9213C>T
|
ENSP00000205890.5:p.Ala3071=
|
|
ENST00000418233.7:c.1005C>T
|
ENSP00000408800.3:p.Ala335=
|
|
ENST00000433411.7:n.150C>T
|
|
|
ENST00000445289.6:n.316+1431C>T
|
|
|
ENST00000556535.5:c.75C>T
|
ENSP00000451782.1:p.Ala25=
|
|
ENST00000557190.5:n.115C>T
|
|
|
ENST00000557655.5:c.75C>T
|
ENSP00000451925.1:p.Ala25=
|
|
ENST00000578472.5:c.75C>T
|
ENSP00000467989.1:p.Ala25=
|
|
ENST00000615845.4:c.9213C>T
|
ENSP00000481642.1:p.Ala3071=
|
|
NM_016239.3:c.9213C>T
|
NP_057323.3:p.Ala3071=
|
|
XM_011523921.1:c.9207C>T
|
XP_011522223.1:p.Ala3069=
|
|
XM_017024714.2:c.9153C>T
|
XP_016880203.1:p.Ala3051=
|
|
XM_017024715.2:c.9216C>T
|
XP_016880204.1:p.Ala3072=
|
|
NM_016239.4:c.9213C>T
MANE Select
|
NP_057323.3:p.Ala3071=
|
|