ENST00000541682.7:c.495G>C
MANE Select
|
ENSP00000446205.2:p.Gln165His
|
|
ENST00000317814.8:c.480G>C
|
ENSP00000314774.4:p.Gln160His
|
|
ENST00000541682.6:c.495G>C
|
ENSP00000446205.2:p.Gln165His
|
|
NM_001165967.1:c.495G>C
|
NP_001159439.1:p.Gln165His
|
|
NM_032580.3:c.480G>C
|
NP_115969.2:p.Gln160His
|
|
XM_011524038.1:c.600G>C
|
XP_011522340.1:p.Gln200His
|
|
XM_011524039.1:c.591G>C
|
XP_011522341.1:p.Gln197His
|
|
XM_011524040.1:c.591G>C
|
XP_011522342.1:p.Gln197His
|
|
XM_011524041.1:c.582G>C
|
XP_011522343.1:p.Gln194His
|
|
XM_011524042.1:c.453G>C
|
XP_011522344.1:p.Gln151His
|
|
XR_934203.1:n.69+1955C>G
|
|
|
XM_017025232.1:c.600G>C
|
XP_016880721.1:p.Gln200His
|
|
XM_024451007.1:c.600G>C
|
XP_024306775.1:p.Gln200His
|
|
NM_001165967.2:c.495G>C
MANE Select
|
NP_001159439.1:p.Gln165His
|
|
NM_032580.4:c.480G>C
|
NP_115969.2:p.Gln160His
|
|