ENST00000478003.2:n.2070C=
|
|
|
ENST00000682276.1:n.1687C=
|
|
|
ENST00000682892.1:c.1789C=
|
ENSP00000507214.1:p.His597=
|
|
ENST00000682952.1:n.1881C=
|
|
|
ENST00000684455.1:c.1455C=
|
|
|
ENST00000684642.1:c.1639C=
|
ENSP00000507355.1:p.His547=
|
|
ENST00000684740.1:n.2420C=
|
|
|
ENST00000303236.9:c.2242C=
MANE Select
|
ENSP00000307235.3:p.His748=
|
|
ENST00000652099.1:c.2436C=
|
|
|
ENST00000652736.1:n.2118C=
|
|
|
ENST00000303236.7:c.2242C=
|
ENSP00000307235.3:p.His748=
|
|
ENST00000415570.1:c.1879C=
|
ENSP00000412076.1:p.His627=
|
|
ENST00000419748.5:c.1789C=
|
ENSP00000408325.1:p.His597=
|
|
ENST00000470706.1:n.48+120C=
|
|
|
NM_001313915.1:c.1789C=
|
NP_001300844.1:p.His597=
|
|
NM_004836.5:c.2242C=
|
NP_004827.4:p.His748=
|
|
NM_004836.6:c.2242C=
|
NP_004827.4:p.His748=
|
|
NR_110236.1:n.1378G=
|
|
|
XM_005264649.3:c.1558C=
|
XP_005264706.1:p.His520=
|
|
XM_017005376.2:c.1558C=
|
XP_016860865.1:p.His520=
|
|
NM_004836.7:c.2242C=
MANE Select
|
NP_004827.4:p.His748=
|
|
NM_001313915.2:c.1789C=
|
NP_001300844.1:p.His597=
|
|