ENST00000350026.11:c.3811A>T
|
ENSP00000055163.8:p.Asn1271Tyr
|
|
ENST00000414678.8:c.3880A>T
|
ENSP00000412835.3:p.Asn1294Tyr
|
|
ENST00000637015.2:c.4099A>T
|
ENSP00000489729.2:p.Asn1367Tyr
|
|
ENST00000346085.10:c.3850A>T
|
ENSP00000344546.5:p.Asn1284Tyr
|
|
ENST00000350026.10:c.3562A>T
|
ENSP00000055163.7:p.Asn1188Tyr
|
|
ENST00000414678.7:c.2128A>T
|
ENSP00000412835.2:p.Asn710Tyr
|
|
ENST00000635849.1:c.1291A>T
|
ENSP00000490948.1:p.Asn431Tyr
|
|
ENST00000635957.1:c.925A>T
|
ENSP00000490385.1:p.Asn309Tyr
|
|
ENST00000636930.2:c.3970A>T
MANE Select
|
ENSP00000490491.2:p.Asn1324Tyr
|
|
ENST00000636940.1:n.1967A>T
|
|
|
ENST00000637015.1:c.1338A>T
|
|
|
ENST00000637568.1:c.1252A>T
|
|
|
ENST00000637741.1:n.636A>T
|
|
|
ENST00000637810.1:c.1312A>T
|
ENSP00000489636.1:p.Asn438Tyr
|
|
ENST00000637904.1:c.1471A>T
|
ENSP00000490550.1:p.Asn491Tyr
|
|
ENST00000647938.1:c.3601A>T
|
ENSP00000498155.1:p.Asn1201Tyr
|
|
ENST00000346085.9:c.3601A>T
|
ENSP00000344546.4:p.Asn1201Tyr
|
|
ENST00000350026.9:c.3562A>T
|
ENSP00000055163.7:p.Asn1188Tyr
|
|
ENST00000414678.6:c.2128A>T
|
ENSP00000412835.2:p.Asn710Tyr
|
|
NM_017519.2:c.3562A>T
|
NP_059989.2:p.Asn1188Tyr
|
|
NM_020732.3:c.3601A>T
|
NP_065783.3:p.Asn1201Tyr
|
|
XM_005267069.3:c.3721A>T
|
XP_005267126.2:p.Asn1241Tyr
|
|
XM_011535984.1:c.2800A>T
|
XP_011534286.1:p.Asn934Tyr
|
|
XM_011535985.1:c.2620A>T
|
XP_011534287.1:p.Asn874Tyr
|
|
XM_011535986.1:c.2380A>T
|
XP_011534288.1:p.Asn794Tyr
|
|
XM_011535987.1:c.1999A>T
|
XP_011534289.1:p.Asn667Tyr
|
|
XM_011535988.1:c.862A>T
|
XP_011534290.1:p.Asn288Tyr
|
|
NM_001346813.1:c.3721A>T
|
NP_001333742.1:p.Asn1241Tyr
|
|
NM_001363725.1:c.1471A>T
|
NP_001350654.1:p.Asn491Tyr
|
|
XM_011535984.2:c.3931A>T
|
XP_011534286.2:p.Asn1311Tyr
|
|
XM_011535988.3:c.862A>T
|
XP_011534290.1:p.Asn288Tyr
|
|
XM_017011103.2:c.3832A>T
|
XP_016866592.1:p.Asn1278Tyr
|
|
XM_017011104.1:c.3802A>T
|
XP_016866593.1:p.Asn1268Tyr
|
|
XM_017011105.2:c.3772A>T
|
XP_016866594.1:p.Asn1258Tyr
|
|
XM_017011106.2:c.3643A>T
|
XP_016866595.1:p.Asn1215Tyr
|
|
XM_017011107.2:c.3622A>T
|
XP_016866596.1:p.Asn1208Tyr
|
|
XR_002956289.1:n.4014A>T
|
|
|
NM_001363725.2:c.1471A>T
|
NP_001350654.1:p.Asn491Tyr
|
|
NM_001371656.1:c.3850A>T
|
NP_001358585.1:p.Asn1284Tyr
|
|
NM_001374820.1:c.3850A>T
|
NP_001361749.1:p.Asn1284Tyr
|
|
NM_001374828.1:c.3970A>T
MANE Select
|
NP_001361757.1:p.Asn1324Tyr
|
|
NM_017519.3:c.3811A>T
|
NP_059989.3:p.Asn1271Tyr
|
|