ENST00000337653.7:c.1660T>G
MANE Select
|
ENSP00000337103.2:p.Tyr554Asp
|
|
ENST00000638282.1:c.*497T>G
|
ENSP00000492646.1:n.*497T>G
|
|
ENST00000638683.1:n.297T>G
|
|
|
ENST00000640822.1:c.523T>G
|
ENSP00000491328.1:p.Tyr175Asp
|
|
ENST00000337653.6:c.1660T>G
|
ENSP00000337103.2:p.Tyr554Asp
|
|
ENST00000339797.5:c.1306T>G
|
ENSP00000343486.1:p.Tyr436Asp
|
|
ENST00000351556.7:c.1306T>G
|
ENSP00000345878.3:p.Tyr436Asp
|
|
ENST00000395559.6:c.1306T>G
|
ENSP00000378926.2:p.Tyr436Asp
|
|
ENST00000395562.2:c.1414T>G
|
ENSP00000378929.2:p.Tyr472Asp
|
|
ENST00000466590.6:c.*1391T>G
|
ENSP00000473443.1:n.*1391T>G
|
|
NM_001142929.1:c.1306T>G
|
NP_001136401.1:p.Tyr436Asp
|
|
NM_001142933.1:c.1414T>G
|
NP_001136405.1:p.Tyr472Asp
|
|
NM_001142934.1:c.1306T>G
|
NP_001136406.1:p.Tyr436Asp
|
|
NM_020549.4:c.1660T>G
|
NP_065574.3:p.Tyr554Asp
|
|
NM_020984.3:c.1306T>G
|
NP_066264.3:p.Tyr436Asp
|
|
NM_020985.3:c.1306T>G
|
NP_066265.3:p.Tyr436Asp
|
|
NM_020986.3:c.1306T>G
|
NP_066266.3:p.Tyr436Asp
|
|
NM_001142929.2:c.1306T>G
|
NP_001136401.2:p.Tyr436Asp
|
|
NM_001142933.2:c.1414T>G
|
NP_001136405.2:p.Tyr472Asp
|
|
NM_001142934.2:c.1306T>G
|
NP_001136406.2:p.Tyr436Asp
|
|
NM_020549.5:c.1660T>G
MANE Select
|
NP_065574.4:p.Tyr554Asp
|
|
NM_020984.4:c.1306T>G
|
NP_066264.4:p.Tyr436Asp
|
|
NM_020985.4:c.1306T>G
|
NP_066265.4:p.Tyr436Asp
|
|
NM_020986.4:c.1306T>G
|
NP_066266.4:p.Tyr436Asp
|
|