ENST00000541682.7:c.382C>G
MANE Select
|
ENSP00000446205.2:p.His128Asp
|
|
ENST00000317814.8:c.367C>G
|
ENSP00000314774.4:p.His123Asp
|
|
ENST00000541682.6:c.382C>G
|
ENSP00000446205.2:p.His128Asp
|
|
ENST00000577735.1:c.358C>G
|
ENSP00000462491.1:p.His120Asp
|
|
NM_001165967.1:c.382C>G
|
NP_001159439.1:p.His128Asp
|
|
NM_032580.3:c.367C>G
|
NP_115969.2:p.His123Asp
|
|
XM_011524038.1:c.487C>G
|
XP_011522340.1:p.His163Asp
|
|
XM_011524039.1:c.478C>G
|
XP_011522341.1:p.His160Asp
|
|
XM_011524040.1:c.478C>G
|
XP_011522342.1:p.His160Asp
|
|
XM_011524041.1:c.469C>G
|
XP_011522343.1:p.His157Asp
|
|
XM_011524042.1:c.340C>G
|
XP_011522344.1:p.His114Asp
|
|
XR_934203.1:n.69+2068G>C
|
|
|
XM_017025232.1:c.487C>G
|
XP_016880721.1:p.His163Asp
|
|
XM_024451007.1:c.487C>G
|
XP_024306775.1:p.His163Asp
|
|
NM_001165967.2:c.382C>G
MANE Select
|
NP_001159439.1:p.His128Asp
|
|
NM_032580.4:c.367C>G
|
NP_115969.2:p.His123Asp
|
|