ENST00000527168.6:n.722T=
|
|
|
ENST00000529110.2:c.707T=
|
ENSP00000435349.2:p.Leu236=
|
|
ENST00000529957.6:n.681T=
|
|
|
ENST00000683366.1:c.*355T=
|
ENSP00000507283.1:n.*355T=
|
|
ENST00000683887.1:c.671T=
|
ENSP00000506886.1:p.Leu224=
|
|
ENST00000684100.1:n.617T=
|
|
|
ENST00000684126.1:n.757T=
|
|
|
ENST00000684688.1:n.1248T=
|
|
|
ENST00000204679.9:c.623T=
MANE Select
|
ENSP00000204679.4:p.Leu208=
|
|
ENST00000204679.8:c.623T=
|
ENSP00000204679.4:p.Leu208=
|
|
ENST00000527076.1:n.1846T=
|
|
|
ENST00000527168.5:n.790T=
|
|
|
ENST00000529957.5:n.722T=
|
|
|
NM_032520.4:c.623T=
|
NP_115909.1:p.Leu208=
|
|
XM_017023782.1:c.671T=
|
XP_016879271.1:p.Leu224=
|
|
XM_017023783.1:c.263T=
|
XP_016879272.1:p.Leu88=
|
|
NM_032520.5:c.623T=
MANE Select
|
NP_115909.1:p.Leu208=
|
|