ENST00000409110.6:c.1193G>C
MANE Select
|
ENSP00000386444.1:p.Arg398Thr
|
|
ENST00000409110.5:c.1193G>C
|
ENSP00000386444.1:p.Arg398Thr
|
|
ENST00000412969.6:n.2413G>C
|
|
|
ENST00000471884.5:n.3224G>C
|
|
|
ENST00000474220.5:n.399G>C
|
|
|
ENST00000476500.5:n.6492G>C
|
|
|
ENST00000492629.1:n.154G>C
|
|
|
NM_000541.4:c.1193G>C
|
NP_000532.2:p.Arg398Thr
|
|
XM_011511589.1:c.1193G>C
|
XP_011509891.1:p.Arg398Thr
|
|
XM_011511590.1:c.1193G>C
|
XP_011509892.1:p.Arg398Thr
|
|
XM_011511591.1:c.*61G>C
|
XP_011509893.1:n.*61G>C
|
|
XM_011511592.1:c.1037G>C
|
XP_011509894.1:p.Arg346Thr
|
|
XM_011511593.1:c.893G>C
|
XP_011509895.1:p.Arg298Thr
|
|
XM_011511594.1:c.821G>C
|
XP_011509896.1:p.Arg274Thr
|
|
XM_011511596.1:c.791G>C
|
XP_011509898.1:p.Arg264Thr
|
|
XM_011511597.1:c.791G>C
|
XP_011509899.1:p.Arg264Thr
|
|
XR_922978.1:n.1510G>C
|
|
|
XR_922980.1:n.1609G>C
|
|
|
XM_011511593.3:c.893G>C
|
XP_011509895.1:p.Arg298Thr
|
|
XM_017004641.1:c.*61G>C
|
XP_016860130.1:n.*61G>C
|
|
XM_024453036.1:c.*61G>C
|
XP_024308804.1:n.*61G>C
|
|
XR_001738882.1:n.1391G>C
|
|
|
XR_922980.2:n.1609G>C
|
|
|
NM_000541.5:c.1193G>C
MANE Select
|
NP_000532.2:p.Arg398Thr
|
|