ENST00000537320.6:c.3856T>G
|
ENSP00000443478.1:p.Ser1286Ala
|
|
ENST00000542877.6:c.4678T>G
|
ENSP00000442242.1:p.Ser1560Ala
|
|
ENST00000705190.1:c.2710T>G
|
ENSP00000516083.1:p.Ser904Ala
|
|
ENST00000705191.1:c.1366T>G
|
ENSP00000516084.1:p.Ser456Ala
|
|
ENST00000705192.1:c.4725T>G
|
|
|
ENST00000350763.9:c.5767T>G
MANE Select
|
ENSP00000265131.4:p.Ser1923Ala
|
|
ENST00000341037.8:c.5221T>G
|
ENSP00000339553.4:p.Ser1741Ala
|
|
ENST00000350763.8:c.5767T>G
|
ENSP00000265131.4:p.Ser1923Ala
|
|
ENST00000423613.6:c.4948T>G
|
ENSP00000411406.2:p.Ser1650Ala
|
|
ENST00000460345.1:n.349T>G
|
|
|
ENST00000535648.5:c.4678T>G
|
ENSP00000438152.2:p.Ser1560Ala
|
|
ENST00000537320.5:c.3856T>G
|
ENSP00000443478.1:p.Ser1286Ala
|
|
ENST00000542877.5:c.4678T>G
|
ENSP00000442242.1:p.Ser1560Ala
|
|
ENST00000544972.1:c.1454T>G
|
|
|
NM_002160.3:c.5767T>G
|
NP_002151.2:p.Ser1923Ala
|
|
XM_005251972.2:c.5494T>G
|
XP_005252029.1:p.Ser1832Ala
|
|
XM_005251973.2:c.4675T>G
|
XP_005252030.1:p.Ser1559Ala
|
|
XM_005251974.2:c.4129T>G
|
XP_005252031.1:p.Ser1377Ala
|
|
XM_005251975.2:c.3856T>G
|
XP_005252032.1:p.Ser1286Ala
|
|
XM_006717096.2:c.6043T>G
|
XP_006717159.1:p.Ser2015Ala
|
|
XM_006717097.2:c.5494T>G
|
XP_006717160.1:p.Ser1832Ala
|
|
XM_006717098.2:c.5221T>G
|
XP_006717161.1:p.Ser1741Ala
|
|
XM_006717100.2:c.4948T>G
|
XP_006717163.1:p.Ser1650Ala
|
|
XM_006717101.2:c.4129T>G
|
XP_006717164.1:p.Ser1377Ala
|
|
XM_011518622.1:c.5770T>G
|
XP_011516924.1:p.Ser1924Ala
|
|
XM_011518623.1:c.5770T>G
|
XP_011516925.1:p.Ser1924Ala
|
|
XM_011518624.1:c.5224T>G
|
XP_011516926.1:p.Ser1742Ala
|
|
XM_011518625.1:c.5221T>G
|
XP_011516927.1:p.Ser1741Ala
|
|
XM_011518626.1:c.4951T>G
|
XP_011516928.1:p.Ser1651Ala
|
|
XM_011518627.1:c.4678T>G
|
XP_011516929.1:p.Ser1560Ala
|
|
XM_011518628.1:c.4402T>G
|
XP_011516930.1:p.Ser1468Ala
|
|
XM_011518629.1:c.4402T>G
|
XP_011516931.1:p.Ser1468Ala
|
|
XM_005251972.4:c.5494T>G
|
XP_005252029.1:p.Ser1832Ala
|
|
XM_005251973.4:c.4675T>G
|
XP_005252030.1:p.Ser1559Ala
|
|
XM_005251974.4:c.4129T>G
|
XP_005252031.1:p.Ser1377Ala
|
|
XM_005251975.4:c.3856T>G
|
XP_005252032.1:p.Ser1286Ala
|
|
XM_006717096.4:c.6043T>G
|
XP_006717159.1:p.Ser2015Ala
|
|
XM_006717097.4:c.5494T>G
|
XP_006717160.1:p.Ser1832Ala
|
|
XM_006717098.4:c.5221T>G
|
XP_006717161.1:p.Ser1741Ala
|
|
XM_006717101.4:c.4129T>G
|
XP_006717164.1:p.Ser1377Ala
|
|
XM_011518625.3:c.5221T>G
|
XP_011516927.1:p.Ser1741Ala
|
|
XM_011518626.3:c.4951T>G
|
XP_011516928.1:p.Ser1651Ala
|
|
XM_011518628.3:c.4402T>G
|
XP_011516930.1:p.Ser1468Ala
|
|
XM_011518629.3:c.4402T>G
|
XP_011516931.1:p.Ser1468Ala
|
|
XM_017014678.2:c.6316T>G
|
XP_016870167.1:p.Ser2106Ala
|
|
XM_017014679.2:c.6043T>G
|
XP_016870168.1:p.Ser2015Ala
|
|
XM_017014680.2:c.6040T>G
|
XP_016870169.1:p.Ser2014Ala
|
|
XM_017014681.2:c.5224T>G
|
XP_016870170.1:p.Ser1742Ala
|
|
XM_024447530.1:c.6316T>G
|
XP_024303298.1:p.Ser2106Ala
|
|
NM_002160.4:c.5767T>G
MANE Select
|
NP_002151.2:p.Ser1923Ala
|
|