ENST00000399503.4:c.2871A>C
MANE Select
|
ENSP00000382423.3:p.Gln957His
|
|
ENST00000399503.3:c.2871A>C
|
ENSP00000382423.3:p.Gln957His
|
|
NM_005921.1:c.2871A>C
|
NP_005912.1:p.Gln957His
|
|
XM_005248519.3:c.2493A>C
|
XP_005248576.2:p.Gln831His
|
|
XM_011543406.1:c.2616A>C
|
XP_011541708.1:p.Gln872His
|
|
XM_011543407.1:c.2592A>C
|
XP_011541709.1:p.Gln864His
|
|
XM_011543408.1:c.2871A>C
|
XP_011541710.1:p.Gln957His
|
|
XM_017009484.1:c.2460A>C
|
XP_016864973.1:p.Gln820His
|
|
XM_017009485.1:c.2382A>C
|
XP_016864974.1:p.Gln794His
|
|
XR_001742068.2:n.2902A>C
|
|
|
NM_005921.2:c.2871A>C
MANE Select
|
NP_005912.1:p.Gln957His
|
|