|
ENST00000350026.11:c.4390A>G
|
ENSP00000055163.8:p.Met1464Val
|
|
|
ENST00000414678.8:c.4459A>G
|
ENSP00000412835.3:p.Met1487Val
|
|
|
ENST00000637015.2:c.4678A>G
|
ENSP00000489729.2:p.Met1560Val
|
|
|
ENST00000346085.10:c.4429A>G
|
ENSP00000344546.5:p.Met1477Val
|
|
|
ENST00000350026.10:c.4141A>G
|
ENSP00000055163.7:p.Met1381Val
|
|
|
ENST00000414678.7:c.2707A>G
|
ENSP00000412835.2:p.Met903Val
|
|
|
ENST00000635849.1:c.1870A>G
|
ENSP00000490948.1:p.Met624Val
|
|
|
ENST00000635957.1:c.1501A>G
|
ENSP00000490385.1:p.Met501Val
|
|
|
ENST00000636227.1:n.3012A>G
|
|
|
|
ENST00000636254.1:n.469A>G
|
|
|
|
ENST00000636930.2:c.4549A>G
MANE Select
|
ENSP00000490491.2:p.Met1517Val
|
|
|
ENST00000636940.1:n.2546A>G
|
|
|
|
ENST00000637015.1:c.1917A>G
|
|
|
|
ENST00000637568.1:c.1831A>G
|
|
|
|
ENST00000637741.1:n.1215A>G
|
|
|
|
ENST00000637810.1:c.1891A>G
|
ENSP00000489636.1:p.Met631Val
|
|
|
ENST00000637904.1:c.2050A>G
|
ENSP00000490550.1:p.Met684Val
|
|
|
ENST00000647938.1:c.4180A>G
|
ENSP00000498155.1:p.Met1394Val
|
|
|
ENST00000346085.9:c.4180A>G
|
ENSP00000344546.4:p.Met1394Val
|
|
|
ENST00000350026.9:c.4141A>G
|
ENSP00000055163.7:p.Met1381Val
|
|
|
ENST00000414678.6:c.2707A>G
|
ENSP00000412835.2:p.Met903Val
|
|
|
NM_017519.2:c.4141A>G
|
NP_059989.2:p.Met1381Val
|
|
|
NM_020732.3:c.4180A>G
|
NP_065783.3:p.Met1394Val
|
|
|
XM_005267069.3:c.4300A>G
|
XP_005267126.2:p.Met1434Val
|
|
|
XM_011535984.1:c.3379A>G
|
XP_011534286.1:p.Met1127Val
|
|
|
XM_011535985.1:c.3199A>G
|
XP_011534287.1:p.Met1067Val
|
|
|
XM_011535986.1:c.2959A>G
|
XP_011534288.1:p.Met987Val
|
|
|
XM_011535987.1:c.2578A>G
|
XP_011534289.1:p.Met860Val
|
|
|
XM_011535988.1:c.1441A>G
|
XP_011534290.1:p.Met481Val
|
|
|
NM_001346813.1:c.4300A>G
|
NP_001333742.1:p.Met1434Val
|
|
|
NM_001363725.1:c.2050A>G
|
NP_001350654.1:p.Met684Val
|
|
|
XM_011535984.2:c.4510A>G
|
XP_011534286.2:p.Met1504Val
|
|
|
XM_011535988.3:c.1441A>G
|
XP_011534290.1:p.Met481Val
|
|
|
XM_017011103.2:c.4411A>G
|
XP_016866592.1:p.Met1471Val
|
|
|
XM_017011104.1:c.4381A>G
|
XP_016866593.1:p.Met1461Val
|
|
|
XM_017011105.2:c.4351A>G
|
XP_016866594.1:p.Met1451Val
|
|
|
XM_017011106.2:c.4222A>G
|
XP_016866595.1:p.Met1408Val
|
|
|
XM_017011107.2:c.4201A>G
|
XP_016866596.1:p.Met1401Val
|
|
|
XR_002956289.1:n.4496A>G
|
|
|
|
NM_001363725.2:c.2050A>G
|
NP_001350654.1:p.Met684Val
|
|
|
NM_001371656.1:c.4429A>G
|
NP_001358585.1:p.Met1477Val
|
|
|
NM_001374820.1:c.4429A>G
|
NP_001361749.1:p.Met1477Val
|
|
|
NM_001374828.1:c.4549A>G
MANE Select
|
NP_001361757.1:p.Met1517Val
|
|
|
NM_017519.3:c.4390A>G
|
NP_059989.3:p.Met1464Val
|
|
