ENST00000350026.11:c.3449T>C
|
ENSP00000055163.8:p.Met1150Thr
|
|
ENST00000414678.8:c.3518T>C
|
ENSP00000412835.3:p.Met1173Thr
|
|
ENST00000637015.2:c.3737T>C
|
ENSP00000489729.2:p.Met1246Thr
|
|
ENST00000319584.11:c.1622T>C
|
ENSP00000313006.7:p.Met541Thr
|
|
ENST00000346085.10:c.3488T>C
|
ENSP00000344546.5:p.Met1163Thr
|
|
ENST00000350026.10:c.3200T>C
|
ENSP00000055163.7:p.Met1067Thr
|
|
ENST00000414678.7:c.1766T>C
|
ENSP00000412835.2:p.Met589Thr
|
|
ENST00000635849.1:c.929T>C
|
ENSP00000490948.1:p.Met310Thr
|
|
ENST00000635957.1:c.563T>C
|
ENSP00000490385.1:p.Met188Thr
|
|
ENST00000636930.2:c.3608T>C
MANE Select
|
ENSP00000490491.2:p.Met1203Thr
|
|
ENST00000636940.1:n.1605T>C
|
|
|
ENST00000637015.1:c.976T>C
|
|
|
ENST00000637568.1:c.890T>C
|
|
|
ENST00000637741.1:n.274T>C
|
|
|
ENST00000637810.1:c.950T>C
|
ENSP00000489636.1:p.Met317Thr
|
|
ENST00000637904.1:c.1109T>C
|
ENSP00000490550.1:p.Met370Thr
|
|
ENST00000647938.1:c.3239T>C
|
ENSP00000498155.1:p.Met1080Thr
|
|
ENST00000319584.10:c.1625T>C
|
ENSP00000313006.6:p.Met542Thr
|
|
ENST00000346085.9:c.3239T>C
|
ENSP00000344546.4:p.Met1080Thr
|
|
ENST00000350026.9:c.3200T>C
|
ENSP00000055163.7:p.Met1067Thr
|
|
ENST00000400790.3:c.401T>C
|
ENSP00000383596.3:p.Met134Thr
|
|
ENST00000414678.6:c.1766T>C
|
ENSP00000412835.2:p.Met589Thr
|
|
ENST00000478761.3:c.810T>C
|
|
|
NM_017519.2:c.3200T>C
|
NP_059989.2:p.Met1067Thr
|
|
NM_020732.3:c.3239T>C
|
NP_065783.3:p.Met1080Thr
|
|
XM_005267069.3:c.3359T>C
|
XP_005267126.2:p.Met1120Thr
|
|
XM_011535984.1:c.2438T>C
|
XP_011534286.1:p.Met813Thr
|
|
XM_011535985.1:c.2258T>C
|
XP_011534287.1:p.Met753Thr
|
|
XM_011535986.1:c.2018T>C
|
XP_011534288.1:p.Met673Thr
|
|
XM_011535987.1:c.1637T>C
|
XP_011534289.1:p.Met546Thr
|
|
XM_011535988.1:c.500T>C
|
XP_011534290.1:p.Met167Thr
|
|
NM_001346813.1:c.3359T>C
|
NP_001333742.1:p.Met1120Thr
|
|
NM_001363725.1:c.1109T>C
|
NP_001350654.1:p.Met370Thr
|
|
XM_011535984.2:c.3569T>C
|
XP_011534286.2:p.Met1190Thr
|
|
XM_011535988.3:c.500T>C
|
XP_011534290.1:p.Met167Thr
|
|
XM_017011103.2:c.3470T>C
|
XP_016866592.1:p.Met1157Thr
|
|
XM_017011104.1:c.3440T>C
|
XP_016866593.1:p.Met1147Thr
|
|
XM_017011105.2:c.3410T>C
|
XP_016866594.1:p.Met1137Thr
|
|
XM_017011106.2:c.3281T>C
|
XP_016866595.1:p.Met1094Thr
|
|
XM_017011107.2:c.3260T>C
|
XP_016866596.1:p.Met1087Thr
|
|
XR_002956289.1:n.3652T>C
|
|
|
NM_001363725.2:c.1109T>C
|
NP_001350654.1:p.Met370Thr
|
|
NM_001371656.1:c.3488T>C
|
NP_001358585.1:p.Met1163Thr
|
|
NM_001374820.1:c.3488T>C
|
NP_001361749.1:p.Met1163Thr
|
|
NM_001374828.1:c.3608T>C
MANE Select
|
NP_001361757.1:p.Met1203Thr
|
|
NM_017519.3:c.3449T>C
|
NP_059989.3:p.Met1150Thr
|
|