ENST00000350026.11:c.3990C>T
|
ENSP00000055163.8:p.Tyr1330=
|
|
ENST00000414678.8:c.4059C>T
|
ENSP00000412835.3:p.Tyr1353=
|
|
ENST00000637015.2:c.4278C>T
|
ENSP00000489729.2:p.Tyr1426=
|
|
ENST00000346085.10:c.4029C>T
|
ENSP00000344546.5:p.Tyr1343=
|
|
ENST00000350026.10:c.3741C>T
|
ENSP00000055163.7:p.Tyr1247=
|
|
ENST00000414678.7:c.2307C>T
|
ENSP00000412835.2:p.Tyr769=
|
|
ENST00000635849.1:c.1470C>T
|
ENSP00000490948.1:p.Tyr490=
|
|
ENST00000635957.1:c.1101C>T
|
ENSP00000490385.1:p.Tyr367=
|
|
ENST00000636930.2:c.4149C>T
MANE Select
|
ENSP00000490491.2:p.Tyr1383=
|
|
ENST00000636940.1:n.2146C>T
|
|
|
ENST00000637015.1:c.1517C>T
|
|
|
ENST00000637568.1:c.1431C>T
|
|
|
ENST00000637741.1:n.815C>T
|
|
|
ENST00000637810.1:c.1491C>T
|
ENSP00000489636.1:p.Tyr497=
|
|
ENST00000637904.1:c.1650C>T
|
ENSP00000490550.1:p.Tyr550=
|
|
ENST00000647938.1:c.3780C>T
|
ENSP00000498155.1:p.Tyr1260=
|
|
ENST00000346085.9:c.3780C>T
|
ENSP00000344546.4:p.Tyr1260=
|
|
ENST00000350026.9:c.3741C>T
|
ENSP00000055163.7:p.Tyr1247=
|
|
ENST00000414678.6:c.2307C>T
|
ENSP00000412835.2:p.Tyr769=
|
|
NM_017519.2:c.3741C>T
|
NP_059989.2:p.Tyr1247=
|
|
NM_020732.3:c.3780C>T
|
NP_065783.3:p.Tyr1260=
|
|
XM_005267069.3:c.3900C>T
|
XP_005267126.2:p.Tyr1300=
|
|
XM_011535984.1:c.2979C>T
|
XP_011534286.1:p.Tyr993=
|
|
XM_011535985.1:c.2799C>T
|
XP_011534287.1:p.Tyr933=
|
|
XM_011535986.1:c.2559C>T
|
XP_011534288.1:p.Tyr853=
|
|
XM_011535987.1:c.2178C>T
|
XP_011534289.1:p.Tyr726=
|
|
XM_011535988.1:c.1041C>T
|
XP_011534290.1:p.Tyr347=
|
|
NM_001346813.1:c.3900C>T
|
NP_001333742.1:p.Tyr1300=
|
|
NM_001363725.1:c.1650C>T
|
NP_001350654.1:p.Tyr550=
|
|
XM_011535984.2:c.4110C>T
|
XP_011534286.2:p.Tyr1370=
|
|
XM_011535988.3:c.1041C>T
|
XP_011534290.1:p.Tyr347=
|
|
XM_017011103.2:c.4011C>T
|
XP_016866592.1:p.Tyr1337=
|
|
XM_017011104.1:c.3981C>T
|
XP_016866593.1:p.Tyr1327=
|
|
XM_017011105.2:c.3951C>T
|
XP_016866594.1:p.Tyr1317=
|
|
XM_017011106.2:c.3822C>T
|
XP_016866595.1:p.Tyr1274=
|
|
XM_017011107.2:c.3801C>T
|
XP_016866596.1:p.Tyr1267=
|
|
XR_002956289.1:n.4193C>T
|
|
|
NM_001363725.2:c.1650C>T
|
NP_001350654.1:p.Tyr550=
|
|
NM_001371656.1:c.4029C>T
|
NP_001358585.1:p.Tyr1343=
|
|
NM_001374820.1:c.4029C>T
|
NP_001361749.1:p.Tyr1343=
|
|
NM_001374828.1:c.4149C>T
MANE Select
|
NP_001361757.1:p.Tyr1383=
|
|
NM_017519.3:c.3990C>T
|
NP_059989.3:p.Tyr1330=
|
|