ENST00000264705.9:c.2419G>C
MANE Select
|
ENSP00000264705.3:p.Asp807His
|
|
ENST00000264705.8:c.2419G>C
|
ENSP00000264705.3:p.Asp807His
|
|
ENST00000403525.5:c.2230G>C
|
ENSP00000384510.1:p.Asp744His
|
|
ENST00000464159.1:n.167G>C
|
|
|
NM_001306079.1:c.2230G>C
|
NP_001293008.1:p.Asp744His
|
|
NM_004341.3:c.2419G>C
|
NP_004332.2:p.Asp807His
|
|
NM_004341.4:c.2419G>C
|
NP_004332.2:p.Asp807His
|
|
XM_005264555.2:c.2419G>C
|
XP_005264612.1:p.Asp807His
|
|
XM_005264556.2:c.2419G>C
|
XP_005264613.1:p.Asp807His
|
|
XM_005264557.2:c.2419G>C
|
XP_005264614.1:p.Asp807His
|
|
XM_006712101.1:c.2230G>C
|
XP_006712164.1:p.Asp744His
|
|
XM_006712101.3:c.2230G>C
|
XP_006712164.1:p.Asp744His
|
|
XM_024453131.1:c.145G>C
|
XP_024308899.1:p.Asp49His
|
|
NM_004341.5:c.2419G>C
MANE Select
|
NP_004332.2:p.Asp807His
|
|
NM_001306079.2:c.2230G>C
|
NP_001293008.1:p.Asp744His
|
|