ENST00000350026.11:c.3972G>T
|
ENSP00000055163.8:p.Met1324Ile
|
|
ENST00000414678.8:c.4041G>T
|
ENSP00000412835.3:p.Met1347Ile
|
|
ENST00000637015.2:c.4260G>T
|
ENSP00000489729.2:p.Met1420Ile
|
|
ENST00000346085.10:c.4011G>T
|
ENSP00000344546.5:p.Met1337Ile
|
|
ENST00000350026.10:c.3723G>T
|
ENSP00000055163.7:p.Met1241Ile
|
|
ENST00000414678.7:c.2289G>T
|
ENSP00000412835.2:p.Met763Ile
|
|
ENST00000635849.1:c.1452G>T
|
ENSP00000490948.1:p.Met484Ile
|
|
ENST00000635957.1:c.1083G>T
|
ENSP00000490385.1:p.Met361Ile
|
|
ENST00000636930.2:c.4131G>T
MANE Select
|
ENSP00000490491.2:p.Met1377Ile
|
|
ENST00000636940.1:n.2128G>T
|
|
|
ENST00000637015.1:c.1499G>T
|
|
|
ENST00000637568.1:c.1413G>T
|
|
|
ENST00000637741.1:n.797G>T
|
|
|
ENST00000637810.1:c.1473G>T
|
ENSP00000489636.1:p.Met491Ile
|
|
ENST00000637904.1:c.1632G>T
|
ENSP00000490550.1:p.Met544Ile
|
|
ENST00000647938.1:c.3762G>T
|
ENSP00000498155.1:p.Met1254Ile
|
|
ENST00000346085.9:c.3762G>T
|
ENSP00000344546.4:p.Met1254Ile
|
|
ENST00000350026.9:c.3723G>T
|
ENSP00000055163.7:p.Met1241Ile
|
|
ENST00000414678.6:c.2289G>T
|
ENSP00000412835.2:p.Met763Ile
|
|
NM_017519.2:c.3723G>T
|
NP_059989.2:p.Met1241Ile
|
|
NM_020732.3:c.3762G>T
|
NP_065783.3:p.Met1254Ile
|
|
XM_005267069.3:c.3882G>T
|
XP_005267126.2:p.Met1294Ile
|
|
XM_011535984.1:c.2961G>T
|
XP_011534286.1:p.Met987Ile
|
|
XM_011535985.1:c.2781G>T
|
XP_011534287.1:p.Met927Ile
|
|
XM_011535986.1:c.2541G>T
|
XP_011534288.1:p.Met847Ile
|
|
XM_011535987.1:c.2160G>T
|
XP_011534289.1:p.Met720Ile
|
|
XM_011535988.1:c.1023G>T
|
XP_011534290.1:p.Met341Ile
|
|
NM_001346813.1:c.3882G>T
|
NP_001333742.1:p.Met1294Ile
|
|
NM_001363725.1:c.1632G>T
|
NP_001350654.1:p.Met544Ile
|
|
XM_011535984.2:c.4092G>T
|
XP_011534286.2:p.Met1364Ile
|
|
XM_011535988.3:c.1023G>T
|
XP_011534290.1:p.Met341Ile
|
|
XM_017011103.2:c.3993G>T
|
XP_016866592.1:p.Met1331Ile
|
|
XM_017011104.1:c.3963G>T
|
XP_016866593.1:p.Met1321Ile
|
|
XM_017011105.2:c.3933G>T
|
XP_016866594.1:p.Met1311Ile
|
|
XM_017011106.2:c.3804G>T
|
XP_016866595.1:p.Met1268Ile
|
|
XM_017011107.2:c.3783G>T
|
XP_016866596.1:p.Met1261Ile
|
|
XR_002956289.1:n.4175G>T
|
|
|
NM_001363725.2:c.1632G>T
|
NP_001350654.1:p.Met544Ile
|
|
NM_001371656.1:c.4011G>T
|
NP_001358585.1:p.Met1337Ile
|
|
NM_001374820.1:c.4011G>T
|
NP_001361749.1:p.Met1337Ile
|
|
NM_001374828.1:c.4131G>T
MANE Select
|
NP_001361757.1:p.Met1377Ile
|
|
NM_017519.3:c.3972G>T
|
NP_059989.3:p.Met1324Ile
|
|