ENST00000350026.11:c.3818T>C
|
ENSP00000055163.8:p.Met1273Thr
|
|
ENST00000414678.8:c.3887T>C
|
ENSP00000412835.3:p.Met1296Thr
|
|
ENST00000637015.2:c.4106T>C
|
ENSP00000489729.2:p.Met1369Thr
|
|
ENST00000346085.10:c.3857T>C
|
ENSP00000344546.5:p.Met1286Thr
|
|
ENST00000350026.10:c.3569T>C
|
ENSP00000055163.7:p.Met1190Thr
|
|
ENST00000414678.7:c.2135T>C
|
ENSP00000412835.2:p.Met712Thr
|
|
ENST00000635849.1:c.1298T>C
|
ENSP00000490948.1:p.Met433Thr
|
|
ENST00000635957.1:c.932T>C
|
ENSP00000490385.1:p.Met311Thr
|
|
ENST00000636930.2:c.3977T>C
MANE Select
|
ENSP00000490491.2:p.Met1326Thr
|
|
ENST00000636940.1:n.1974T>C
|
|
|
ENST00000637015.1:c.1345T>C
|
|
|
ENST00000637568.1:c.1259T>C
|
|
|
ENST00000637741.1:n.643T>C
|
|
|
ENST00000637810.1:c.1319T>C
|
ENSP00000489636.1:p.Met440Thr
|
|
ENST00000637904.1:c.1478T>C
|
ENSP00000490550.1:p.Met493Thr
|
|
ENST00000647938.1:c.3608T>C
|
ENSP00000498155.1:p.Met1203Thr
|
|
ENST00000346085.9:c.3608T>C
|
ENSP00000344546.4:p.Met1203Thr
|
|
ENST00000350026.9:c.3569T>C
|
ENSP00000055163.7:p.Met1190Thr
|
|
ENST00000414678.6:c.2135T>C
|
ENSP00000412835.2:p.Met712Thr
|
|
NM_017519.2:c.3569T>C
|
NP_059989.2:p.Met1190Thr
|
|
NM_020732.3:c.3608T>C
|
NP_065783.3:p.Met1203Thr
|
|
XM_005267069.3:c.3728T>C
|
XP_005267126.2:p.Met1243Thr
|
|
XM_011535984.1:c.2807T>C
|
XP_011534286.1:p.Met936Thr
|
|
XM_011535985.1:c.2627T>C
|
XP_011534287.1:p.Met876Thr
|
|
XM_011535986.1:c.2387T>C
|
XP_011534288.1:p.Met796Thr
|
|
XM_011535987.1:c.2006T>C
|
XP_011534289.1:p.Met669Thr
|
|
XM_011535988.1:c.869T>C
|
XP_011534290.1:p.Met290Thr
|
|
NM_001346813.1:c.3728T>C
|
NP_001333742.1:p.Met1243Thr
|
|
NM_001363725.1:c.1478T>C
|
NP_001350654.1:p.Met493Thr
|
|
XM_011535984.2:c.3938T>C
|
XP_011534286.2:p.Met1313Thr
|
|
XM_011535988.3:c.869T>C
|
XP_011534290.1:p.Met290Thr
|
|
XM_017011103.2:c.3839T>C
|
XP_016866592.1:p.Met1280Thr
|
|
XM_017011104.1:c.3809T>C
|
XP_016866593.1:p.Met1270Thr
|
|
XM_017011105.2:c.3779T>C
|
XP_016866594.1:p.Met1260Thr
|
|
XM_017011106.2:c.3650T>C
|
XP_016866595.1:p.Met1217Thr
|
|
XM_017011107.2:c.3629T>C
|
XP_016866596.1:p.Met1210Thr
|
|
XR_002956289.1:n.4021T>C
|
|
|
NM_001363725.2:c.1478T>C
|
NP_001350654.1:p.Met493Thr
|
|
NM_001371656.1:c.3857T>C
|
NP_001358585.1:p.Met1286Thr
|
|
NM_001374820.1:c.3857T>C
|
NP_001361749.1:p.Met1286Thr
|
|
NM_001374828.1:c.3977T>C
MANE Select
|
NP_001361757.1:p.Met1326Thr
|
|
NM_017519.3:c.3818T>C
|
NP_059989.3:p.Met1273Thr
|
|