ENST00000478003.2:n.2267T>G
|
|
|
ENST00000682276.1:n.1884T>G
|
|
|
ENST00000682892.1:c.1986T>G
|
ENSP00000507214.1:p.Cys662Trp
|
|
ENST00000682952.1:n.2078T>G
|
|
|
ENST00000684455.1:c.1652T>G
|
|
|
ENST00000684642.1:c.1836T>G
|
ENSP00000507355.1:p.Cys612Trp
|
|
ENST00000684740.1:n.2617T>G
|
|
|
ENST00000303236.9:c.2439T>G
MANE Select
|
ENSP00000307235.3:p.Cys813Trp
|
|
ENST00000652099.1:c.2633T>G
|
|
|
ENST00000652736.1:n.2315T>G
|
|
|
ENST00000303236.7:c.2439T>G
|
ENSP00000307235.3:p.Cys813Trp
|
|
ENST00000415570.1:c.2076T>G
|
ENSP00000412076.1:p.Cys692Trp
|
|
ENST00000419748.5:c.1986T>G
|
ENSP00000408325.1:p.Cys662Trp
|
|
ENST00000470706.1:n.82T>G
|
|
|
NM_001313915.1:c.1986T>G
|
NP_001300844.1:p.Cys662Trp
|
|
NM_004836.5:c.2439T>G
|
NP_004827.4:p.Cys813Trp
|
|
NM_004836.6:c.2439T>G
|
NP_004827.4:p.Cys813Trp
|
|
NR_110236.1:n.1181A>C
|
|
|
XM_005264649.3:c.1755T>G
|
XP_005264706.1:p.Cys585Trp
|
|
XM_017005376.2:c.1755T>G
|
XP_016860865.1:p.Cys585Trp
|
|
NM_004836.7:c.2439T>G
MANE Select
|
NP_004827.4:p.Cys813Trp
|
|
NM_001313915.2:c.1986T>G
|
NP_001300844.1:p.Cys662Trp
|
|