ENST00000409110.6:c.1126A>C
MANE Select
|
ENSP00000386444.1:p.Asn376His
|
|
ENST00000409110.5:c.1126A>C
|
ENSP00000386444.1:p.Asn376His
|
|
ENST00000412969.6:n.2346A>C
|
|
|
ENST00000471884.5:n.3157A>C
|
|
|
ENST00000474220.5:n.332A>C
|
|
|
ENST00000476500.5:n.6425A>C
|
|
|
ENST00000492629.1:n.87A>C
|
|
|
NM_000541.4:c.1126A>C
|
NP_000532.2:p.Asn376His
|
|
XM_011511589.1:c.1126A>C
|
XP_011509891.1:p.Asn376His
|
|
XM_011511590.1:c.1126A>C
|
XP_011509892.1:p.Asn376His
|
|
XM_011511591.1:c.1116A>C
|
XP_011509893.1:p.Gln372His
|
|
XM_011511592.1:c.970A>C
|
XP_011509894.1:p.Asn324His
|
|
XM_011511593.1:c.826A>C
|
XP_011509895.1:p.Asn276His
|
|
XM_011511594.1:c.754A>C
|
XP_011509896.1:p.Asn252His
|
|
XM_011511596.1:c.724A>C
|
XP_011509898.1:p.Asn242His
|
|
XM_011511597.1:c.724A>C
|
XP_011509899.1:p.Asn242His
|
|
XR_922978.1:n.1443A>C
|
|
|
XR_922979.1:n.1447A>C
|
|
|
XR_922980.1:n.1542A>C
|
|
|
XM_011511593.3:c.826A>C
|
XP_011509895.1:p.Asn276His
|
|
XM_017004641.1:c.1116A>C
|
XP_016860130.1:p.Gln372His
|
|
XM_024453036.1:c.714A>C
|
XP_024308804.1:p.Gln238His
|
|
XR_001738882.1:n.1324A>C
|
|
|
XR_922980.2:n.1542A>C
|
|
|
NM_000541.5:c.1126A>C
MANE Select
|
NP_000532.2:p.Asn376His
|
|