ENST00000350026.11:c.4634A>T
|
ENSP00000055163.8:p.Tyr1545Phe
|
|
ENST00000414678.8:c.4703A>T
|
ENSP00000412835.3:p.Tyr1568Phe
|
|
ENST00000637015.2:c.4922A>T
|
ENSP00000489729.2:p.Tyr1641Phe
|
|
ENST00000346085.10:c.4673A>T
|
ENSP00000344546.5:p.Tyr1558Phe
|
|
ENST00000350026.10:c.4385A>T
|
ENSP00000055163.7:p.Tyr1462Phe
|
|
ENST00000414678.7:c.2951A>T
|
ENSP00000412835.2:p.Tyr984Phe
|
|
ENST00000635849.1:c.2114A>T
|
ENSP00000490948.1:p.Tyr705Phe
|
|
ENST00000635957.1:c.1745A>T
|
ENSP00000490385.1:p.Tyr582Phe
|
|
ENST00000636227.1:n.3256A>T
|
|
|
ENST00000636254.1:n.713A>T
|
|
|
ENST00000636930.2:c.4793A>T
MANE Select
|
ENSP00000490491.2:p.Tyr1598Phe
|
|
ENST00000636940.1:n.2790A>T
|
|
|
ENST00000637015.1:c.2161A>T
|
|
|
ENST00000637568.1:c.2075A>T
|
|
|
ENST00000637741.1:n.1459A>T
|
|
|
ENST00000637810.1:c.2135A>T
|
ENSP00000489636.1:p.Tyr712Phe
|
|
ENST00000637904.1:c.2294A>T
|
ENSP00000490550.1:p.Tyr765Phe
|
|
ENST00000647938.1:c.4424A>T
|
ENSP00000498155.1:p.Tyr1475Phe
|
|
ENST00000346085.9:c.4424A>T
|
ENSP00000344546.4:p.Tyr1475Phe
|
|
ENST00000350026.9:c.4385A>T
|
ENSP00000055163.7:p.Tyr1462Phe
|
|
ENST00000414678.6:c.2951A>T
|
ENSP00000412835.2:p.Tyr984Phe
|
|
NM_017519.2:c.4385A>T
|
NP_059989.2:p.Tyr1462Phe
|
|
NM_020732.3:c.4424A>T
|
NP_065783.3:p.Tyr1475Phe
|
|
XM_005267069.3:c.4544A>T
|
XP_005267126.2:p.Tyr1515Phe
|
|
XM_011535984.1:c.3623A>T
|
XP_011534286.1:p.Tyr1208Phe
|
|
XM_011535985.1:c.3443A>T
|
XP_011534287.1:p.Tyr1148Phe
|
|
XM_011535986.1:c.3203A>T
|
XP_011534288.1:p.Tyr1068Phe
|
|
XM_011535987.1:c.2822A>T
|
XP_011534289.1:p.Tyr941Phe
|
|
XM_011535988.1:c.1685A>T
|
XP_011534290.1:p.Tyr562Phe
|
|
NM_001346813.1:c.4544A>T
|
NP_001333742.1:p.Tyr1515Phe
|
|
NM_001363725.1:c.2294A>T
|
NP_001350654.1:p.Tyr765Phe
|
|
XM_011535984.2:c.4754A>T
|
XP_011534286.2:p.Tyr1585Phe
|
|
XM_011535988.3:c.1685A>T
|
XP_011534290.1:p.Tyr562Phe
|
|
XM_017011103.2:c.4655A>T
|
XP_016866592.1:p.Tyr1552Phe
|
|
XM_017011104.1:c.4625A>T
|
XP_016866593.1:p.Tyr1542Phe
|
|
XM_017011105.2:c.4595A>T
|
XP_016866594.1:p.Tyr1532Phe
|
|
XM_017011106.2:c.4466A>T
|
XP_016866595.1:p.Tyr1489Phe
|
|
XM_017011107.2:c.4445A>T
|
XP_016866596.1:p.Tyr1482Phe
|
|
XR_002956289.1:n.4740A>T
|
|
|
NM_001363725.2:c.2294A>T
|
NP_001350654.1:p.Tyr765Phe
|
|
NM_001371656.1:c.4673A>T
|
NP_001358585.1:p.Tyr1558Phe
|
|
NM_001374820.1:c.4673A>T
|
NP_001361749.1:p.Tyr1558Phe
|
|
NM_001374828.1:c.4793A>T
MANE Select
|
NP_001361757.1:p.Tyr1598Phe
|
|
NM_017519.3:c.4634A>T
|
NP_059989.3:p.Tyr1545Phe
|
|