ENST00000350026.11:c.4909A>G
|
ENSP00000055163.8:p.Met1637Val
|
|
ENST00000414678.8:c.4978A>G
|
ENSP00000412835.3:p.Met1660Val
|
|
ENST00000637015.2:c.5197A>G
|
ENSP00000489729.2:p.Met1733Val
|
|
ENST00000346085.10:c.4948A>G
|
ENSP00000344546.5:p.Met1650Val
|
|
ENST00000350026.10:c.4660A>G
|
ENSP00000055163.7:p.Met1554Val
|
|
ENST00000414678.7:c.3226A>G
|
ENSP00000412835.2:p.Met1076Val
|
|
ENST00000635849.1:c.2389A>G
|
ENSP00000490948.1:p.Met797Val
|
|
ENST00000635957.1:c.2020A>G
|
ENSP00000490385.1:p.Met674Val
|
|
ENST00000636227.1:n.3531A>G
|
|
|
ENST00000636254.1:n.988A>G
|
|
|
ENST00000636930.2:c.5068A>G
MANE Select
|
ENSP00000490491.2:p.Met1690Val
|
|
ENST00000636940.1:n.3065A>G
|
|
|
ENST00000637015.1:c.2436A>G
|
|
|
ENST00000637568.1:c.2350A>G
|
|
|
ENST00000637741.1:n.1734A>G
|
|
|
ENST00000637810.1:c.2410A>G
|
ENSP00000489636.1:p.Met804Val
|
|
ENST00000637904.1:c.2569A>G
|
ENSP00000490550.1:p.Met857Val
|
|
ENST00000647938.1:c.4699A>G
|
ENSP00000498155.1:p.Met1567Val
|
|
ENST00000346085.9:c.4699A>G
|
ENSP00000344546.4:p.Met1567Val
|
|
ENST00000350026.9:c.4660A>G
|
ENSP00000055163.7:p.Met1554Val
|
|
ENST00000414678.6:c.3226A>G
|
ENSP00000412835.2:p.Met1076Val
|
|
NM_017519.2:c.4660A>G
|
NP_059989.2:p.Met1554Val
|
|
NM_020732.3:c.4699A>G
|
NP_065783.3:p.Met1567Val
|
|
XM_005267069.3:c.4819A>G
|
XP_005267126.2:p.Met1607Val
|
|
XM_011535984.1:c.3898A>G
|
XP_011534286.1:p.Met1300Val
|
|
XM_011535985.1:c.3718A>G
|
XP_011534287.1:p.Met1240Val
|
|
XM_011535986.1:c.3478A>G
|
XP_011534288.1:p.Met1160Val
|
|
XM_011535987.1:c.3097A>G
|
XP_011534289.1:p.Met1033Val
|
|
XM_011535988.1:c.1960A>G
|
XP_011534290.1:p.Met654Val
|
|
NM_001346813.1:c.4819A>G
|
NP_001333742.1:p.Met1607Val
|
|
NM_001363725.1:c.2569A>G
|
NP_001350654.1:p.Met857Val
|
|
XM_011535984.2:c.5029A>G
|
XP_011534286.2:p.Met1677Val
|
|
XM_011535988.3:c.1960A>G
|
XP_011534290.1:p.Met654Val
|
|
XM_017011103.2:c.4930A>G
|
XP_016866592.1:p.Met1644Val
|
|
XM_017011104.1:c.4900A>G
|
XP_016866593.1:p.Met1634Val
|
|
XM_017011105.2:c.4870A>G
|
XP_016866594.1:p.Met1624Val
|
|
XM_017011106.2:c.4741A>G
|
XP_016866595.1:p.Met1581Val
|
|
XM_017011107.2:c.4720A>G
|
XP_016866596.1:p.Met1574Val
|
|
XR_002956289.1:n.5015A>G
|
|
|
NM_001363725.2:c.2569A>G
|
NP_001350654.1:p.Met857Val
|
|
NM_001371656.1:c.4948A>G
|
NP_001358585.1:p.Met1650Val
|
|
NM_001374820.1:c.4948A>G
|
NP_001361749.1:p.Met1650Val
|
|
NM_001374828.1:c.5068A>G
MANE Select
|
NP_001361757.1:p.Met1690Val
|
|
NM_017519.3:c.4909A>G
|
NP_059989.3:p.Met1637Val
|
|