ENST00000478003.2:n.2064A>C
|
|
|
ENST00000682276.1:n.1681A>C
|
|
|
ENST00000682892.1:c.1783A>C
|
ENSP00000507214.1:p.Met595Leu
|
|
ENST00000682952.1:n.1875A>C
|
|
|
ENST00000684455.1:c.1449A>C
|
|
|
ENST00000684642.1:c.1633A>C
|
ENSP00000507355.1:p.Met545Leu
|
|
ENST00000684740.1:n.2414A>C
|
|
|
ENST00000303236.9:c.2236A>C
MANE Select
|
ENSP00000307235.3:p.Met746Leu
|
|
ENST00000652099.1:c.2430A>C
|
|
|
ENST00000652736.1:n.2112A>C
|
|
|
ENST00000303236.7:c.2236A>C
|
ENSP00000307235.3:p.Met746Leu
|
|
ENST00000415570.1:c.1873A>C
|
ENSP00000412076.1:p.Met625Leu
|
|
ENST00000419748.5:c.1783A>C
|
ENSP00000408325.1:p.Met595Leu
|
|
ENST00000470706.1:n.48+114A>C
|
|
|
NM_001313915.1:c.1783A>C
|
NP_001300844.1:p.Met595Leu
|
|
NM_004836.5:c.2236A>C
|
NP_004827.4:p.Met746Leu
|
|
NM_004836.6:c.2236A>C
|
NP_004827.4:p.Met746Leu
|
|
NR_110236.1:n.1384T>G
|
|
|
XM_005264649.3:c.1552A>C
|
XP_005264706.1:p.Met518Leu
|
|
XM_017005376.2:c.1552A>C
|
XP_016860865.1:p.Met518Leu
|
|
NM_004836.7:c.2236A>C
MANE Select
|
NP_004827.4:p.Met746Leu
|
|
NM_001313915.2:c.1783A>C
|
NP_001300844.1:p.Met595Leu
|
|