ENST00000350026.11:c.3988T>C
|
ENSP00000055163.8:p.Tyr1330His
|
|
ENST00000414678.8:c.4057T>C
|
ENSP00000412835.3:p.Tyr1353His
|
|
ENST00000637015.2:c.4276T>C
|
ENSP00000489729.2:p.Tyr1426His
|
|
ENST00000346085.10:c.4027T>C
|
ENSP00000344546.5:p.Tyr1343His
|
|
ENST00000350026.10:c.3739T>C
|
ENSP00000055163.7:p.Tyr1247His
|
|
ENST00000414678.7:c.2305T>C
|
ENSP00000412835.2:p.Tyr769His
|
|
ENST00000635849.1:c.1468T>C
|
ENSP00000490948.1:p.Tyr490His
|
|
ENST00000635957.1:c.1099T>C
|
ENSP00000490385.1:p.Tyr367His
|
|
ENST00000636930.2:c.4147T>C
MANE Select
|
ENSP00000490491.2:p.Tyr1383His
|
|
ENST00000636940.1:n.2144T>C
|
|
|
ENST00000637015.1:c.1515T>C
|
|
|
ENST00000637568.1:c.1429T>C
|
|
|
ENST00000637741.1:n.813T>C
|
|
|
ENST00000637810.1:c.1489T>C
|
ENSP00000489636.1:p.Tyr497His
|
|
ENST00000637904.1:c.1648T>C
|
ENSP00000490550.1:p.Tyr550His
|
|
ENST00000647938.1:c.3778T>C
|
ENSP00000498155.1:p.Tyr1260His
|
|
ENST00000346085.9:c.3778T>C
|
ENSP00000344546.4:p.Tyr1260His
|
|
ENST00000350026.9:c.3739T>C
|
ENSP00000055163.7:p.Tyr1247His
|
|
ENST00000414678.6:c.2305T>C
|
ENSP00000412835.2:p.Tyr769His
|
|
NM_017519.2:c.3739T>C
|
NP_059989.2:p.Tyr1247His
|
|
NM_020732.3:c.3778T>C
|
NP_065783.3:p.Tyr1260His
|
|
XM_005267069.3:c.3898T>C
|
XP_005267126.2:p.Tyr1300His
|
|
XM_011535984.1:c.2977T>C
|
XP_011534286.1:p.Tyr993His
|
|
XM_011535985.1:c.2797T>C
|
XP_011534287.1:p.Tyr933His
|
|
XM_011535986.1:c.2557T>C
|
XP_011534288.1:p.Tyr853His
|
|
XM_011535987.1:c.2176T>C
|
XP_011534289.1:p.Tyr726His
|
|
XM_011535988.1:c.1039T>C
|
XP_011534290.1:p.Tyr347His
|
|
NM_001346813.1:c.3898T>C
|
NP_001333742.1:p.Tyr1300His
|
|
NM_001363725.1:c.1648T>C
|
NP_001350654.1:p.Tyr550His
|
|
XM_011535984.2:c.4108T>C
|
XP_011534286.2:p.Tyr1370His
|
|
XM_011535988.3:c.1039T>C
|
XP_011534290.1:p.Tyr347His
|
|
XM_017011103.2:c.4009T>C
|
XP_016866592.1:p.Tyr1337His
|
|
XM_017011104.1:c.3979T>C
|
XP_016866593.1:p.Tyr1327His
|
|
XM_017011105.2:c.3949T>C
|
XP_016866594.1:p.Tyr1317His
|
|
XM_017011106.2:c.3820T>C
|
XP_016866595.1:p.Tyr1274His
|
|
XM_017011107.2:c.3799T>C
|
XP_016866596.1:p.Tyr1267His
|
|
XR_002956289.1:n.4191T>C
|
|
|
NM_001363725.2:c.1648T>C
|
NP_001350654.1:p.Tyr550His
|
|
NM_001371656.1:c.4027T>C
|
NP_001358585.1:p.Tyr1343His
|
|
NM_001374820.1:c.4027T>C
|
NP_001361749.1:p.Tyr1343His
|
|
NM_001374828.1:c.4147T>C
MANE Select
|
NP_001361757.1:p.Tyr1383His
|
|
NM_017519.3:c.3988T>C
|
NP_059989.3:p.Tyr1330His
|
|