ENST00000350026.11:c.4707G>T
|
ENSP00000055163.8:p.Met1569Ile
|
|
ENST00000414678.8:c.4776G>T
|
ENSP00000412835.3:p.Met1592Ile
|
|
ENST00000637015.2:c.4995G>T
|
ENSP00000489729.2:p.Met1665Ile
|
|
ENST00000346085.10:c.4746G>T
|
ENSP00000344546.5:p.Met1582Ile
|
|
ENST00000350026.10:c.4458G>T
|
ENSP00000055163.7:p.Met1486Ile
|
|
ENST00000414678.7:c.3024G>T
|
ENSP00000412835.2:p.Met1008Ile
|
|
ENST00000635849.1:c.2187G>T
|
ENSP00000490948.1:p.Met729Ile
|
|
ENST00000635957.1:c.1818G>T
|
ENSP00000490385.1:p.Met606Ile
|
|
ENST00000636227.1:n.3329G>T
|
|
|
ENST00000636254.1:n.786G>T
|
|
|
ENST00000636930.2:c.4866G>T
MANE Select
|
ENSP00000490491.2:p.Met1622Ile
|
|
ENST00000636940.1:n.2863G>T
|
|
|
ENST00000637015.1:c.2234G>T
|
|
|
ENST00000637568.1:c.2148G>T
|
|
|
ENST00000637741.1:n.1532G>T
|
|
|
ENST00000637810.1:c.2208G>T
|
ENSP00000489636.1:p.Met736Ile
|
|
ENST00000637904.1:c.2367G>T
|
ENSP00000490550.1:p.Met789Ile
|
|
ENST00000647938.1:c.4497G>T
|
ENSP00000498155.1:p.Met1499Ile
|
|
ENST00000346085.9:c.4497G>T
|
ENSP00000344546.4:p.Met1499Ile
|
|
ENST00000350026.9:c.4458G>T
|
ENSP00000055163.7:p.Met1486Ile
|
|
ENST00000414678.6:c.3024G>T
|
ENSP00000412835.2:p.Met1008Ile
|
|
NM_017519.2:c.4458G>T
|
NP_059989.2:p.Met1486Ile
|
|
NM_020732.3:c.4497G>T
|
NP_065783.3:p.Met1499Ile
|
|
XM_005267069.3:c.4617G>T
|
XP_005267126.2:p.Met1539Ile
|
|
XM_011535984.1:c.3696G>T
|
XP_011534286.1:p.Met1232Ile
|
|
XM_011535985.1:c.3516G>T
|
XP_011534287.1:p.Met1172Ile
|
|
XM_011535986.1:c.3276G>T
|
XP_011534288.1:p.Met1092Ile
|
|
XM_011535987.1:c.2895G>T
|
XP_011534289.1:p.Met965Ile
|
|
XM_011535988.1:c.1758G>T
|
XP_011534290.1:p.Met586Ile
|
|
NM_001346813.1:c.4617G>T
|
NP_001333742.1:p.Met1539Ile
|
|
NM_001363725.1:c.2367G>T
|
NP_001350654.1:p.Met789Ile
|
|
XM_011535984.2:c.4827G>T
|
XP_011534286.2:p.Met1609Ile
|
|
XM_011535988.3:c.1758G>T
|
XP_011534290.1:p.Met586Ile
|
|
XM_017011103.2:c.4728G>T
|
XP_016866592.1:p.Met1576Ile
|
|
XM_017011104.1:c.4698G>T
|
XP_016866593.1:p.Met1566Ile
|
|
XM_017011105.2:c.4668G>T
|
XP_016866594.1:p.Met1556Ile
|
|
XM_017011106.2:c.4539G>T
|
XP_016866595.1:p.Met1513Ile
|
|
XM_017011107.2:c.4518G>T
|
XP_016866596.1:p.Met1506Ile
|
|
XR_002956289.1:n.4813G>T
|
|
|
NM_001363725.2:c.2367G>T
|
NP_001350654.1:p.Met789Ile
|
|
NM_001371656.1:c.4746G>T
|
NP_001358585.1:p.Met1582Ile
|
|
NM_001374820.1:c.4746G>T
|
NP_001361749.1:p.Met1582Ile
|
|
NM_001374828.1:c.4866G>T
MANE Select
|
NP_001361757.1:p.Met1622Ile
|
|
NM_017519.3:c.4707G>T
|
NP_059989.3:p.Met1569Ile
|
|