ENST00000478003.2:n.1911G>C
|
|
|
ENST00000682276.1:n.1528G>C
|
|
|
ENST00000682892.1:c.1630G>C
|
ENSP00000507214.1:p.Val544Leu
|
|
ENST00000682952.1:n.1722G>C
|
|
|
ENST00000684455.1:c.1296G>C
|
|
|
ENST00000684642.1:c.1480G>C
|
ENSP00000507355.1:p.Val494Leu
|
|
ENST00000684740.1:n.2261G>C
|
|
|
ENST00000303236.9:c.2083G>C
MANE Select
|
ENSP00000307235.3:p.Val695Leu
|
|
ENST00000652099.1:c.2277G>C
|
|
|
ENST00000652736.1:n.1959G>C
|
|
|
ENST00000303236.7:c.2083G>C
|
ENSP00000307235.3:p.Val695Leu
|
|
ENST00000415570.1:c.1720G>C
|
ENSP00000412076.1:p.Val574Leu
|
|
ENST00000419748.5:c.1630G>C
|
ENSP00000408325.1:p.Val544Leu
|
|
ENST00000470706.1:n.9G>C
|
|
|
ENST00000478003.1:n.649G>C
|
|
|
NM_001313915.1:c.1630G>C
|
NP_001300844.1:p.Val544Leu
|
|
NM_004836.5:c.2083G>C
|
NP_004827.4:p.Val695Leu
|
|
NM_004836.6:c.2083G>C
|
NP_004827.4:p.Val695Leu
|
|
NR_110236.1:n.1537C>G
|
|
|
XM_005264649.3:c.1399G>C
|
XP_005264706.1:p.Val467Leu
|
|
XR_939749.1:n.2362G>C
|
|
|
XM_017005376.2:c.1399G>C
|
XP_016860865.1:p.Val467Leu
|
|
NM_004836.7:c.2083G>C
MANE Select
|
NP_004827.4:p.Val695Leu
|
|
NM_001313915.2:c.1630G>C
|
NP_001300844.1:p.Val544Leu
|
|