ENST00000350026.11:c.4391T>A
|
ENSP00000055163.8:p.Met1464Lys
|
|
ENST00000414678.8:c.4460T>A
|
ENSP00000412835.3:p.Met1487Lys
|
|
ENST00000637015.2:c.4679T>A
|
ENSP00000489729.2:p.Met1560Lys
|
|
ENST00000346085.10:c.4430T>A
|
ENSP00000344546.5:p.Met1477Lys
|
|
ENST00000350026.10:c.4142T>A
|
ENSP00000055163.7:p.Met1381Lys
|
|
ENST00000414678.7:c.2708T>A
|
ENSP00000412835.2:p.Met903Lys
|
|
ENST00000635849.1:c.1871T>A
|
ENSP00000490948.1:p.Met624Lys
|
|
ENST00000635957.1:c.1502T>A
|
ENSP00000490385.1:p.Met501Lys
|
|
ENST00000636227.1:n.3013T>A
|
|
|
ENST00000636254.1:n.470T>A
|
|
|
ENST00000636930.2:c.4550T>A
MANE Select
|
ENSP00000490491.2:p.Met1517Lys
|
|
ENST00000636940.1:n.2547T>A
|
|
|
ENST00000637015.1:c.1918T>A
|
|
|
ENST00000637568.1:c.1832T>A
|
|
|
ENST00000637741.1:n.1216T>A
|
|
|
ENST00000637810.1:c.1892T>A
|
ENSP00000489636.1:p.Met631Lys
|
|
ENST00000637904.1:c.2051T>A
|
ENSP00000490550.1:p.Met684Lys
|
|
ENST00000647938.1:c.4181T>A
|
ENSP00000498155.1:p.Met1394Lys
|
|
ENST00000346085.9:c.4181T>A
|
ENSP00000344546.4:p.Met1394Lys
|
|
ENST00000350026.9:c.4142T>A
|
ENSP00000055163.7:p.Met1381Lys
|
|
ENST00000414678.6:c.2708T>A
|
ENSP00000412835.2:p.Met903Lys
|
|
NM_017519.2:c.4142T>A
|
NP_059989.2:p.Met1381Lys
|
|
NM_020732.3:c.4181T>A
|
NP_065783.3:p.Met1394Lys
|
|
XM_005267069.3:c.4301T>A
|
XP_005267126.2:p.Met1434Lys
|
|
XM_011535984.1:c.3380T>A
|
XP_011534286.1:p.Met1127Lys
|
|
XM_011535985.1:c.3200T>A
|
XP_011534287.1:p.Met1067Lys
|
|
XM_011535986.1:c.2960T>A
|
XP_011534288.1:p.Met987Lys
|
|
XM_011535987.1:c.2579T>A
|
XP_011534289.1:p.Met860Lys
|
|
XM_011535988.1:c.1442T>A
|
XP_011534290.1:p.Met481Lys
|
|
NM_001346813.1:c.4301T>A
|
NP_001333742.1:p.Met1434Lys
|
|
NM_001363725.1:c.2051T>A
|
NP_001350654.1:p.Met684Lys
|
|
XM_011535984.2:c.4511T>A
|
XP_011534286.2:p.Met1504Lys
|
|
XM_011535988.3:c.1442T>A
|
XP_011534290.1:p.Met481Lys
|
|
XM_017011103.2:c.4412T>A
|
XP_016866592.1:p.Met1471Lys
|
|
XM_017011104.1:c.4382T>A
|
XP_016866593.1:p.Met1461Lys
|
|
XM_017011105.2:c.4352T>A
|
XP_016866594.1:p.Met1451Lys
|
|
XM_017011106.2:c.4223T>A
|
XP_016866595.1:p.Met1408Lys
|
|
XM_017011107.2:c.4202T>A
|
XP_016866596.1:p.Met1401Lys
|
|
XR_002956289.1:n.4497T>A
|
|
|
NM_001363725.2:c.2051T>A
|
NP_001350654.1:p.Met684Lys
|
|
NM_001371656.1:c.4430T>A
|
NP_001358585.1:p.Met1477Lys
|
|
NM_001374820.1:c.4430T>A
|
NP_001361749.1:p.Met1477Lys
|
|
NM_001374828.1:c.4550T>A
MANE Select
|
NP_001361757.1:p.Met1517Lys
|
|
NM_017519.3:c.4391T>A
|
NP_059989.3:p.Met1464Lys
|
|