ENST00000399503.4:c.2720A>G
MANE Select
|
ENSP00000382423.3:p.His907Arg
|
|
ENST00000399503.3:c.2720A>G
|
ENSP00000382423.3:p.His907Arg
|
|
NM_005921.1:c.2720A>G
|
NP_005912.1:p.His907Arg
|
|
XM_005248519.3:c.2342A>G
|
XP_005248576.2:p.His781Arg
|
|
XM_011543406.1:c.2465A>G
|
XP_011541708.1:p.His822Arg
|
|
XM_011543407.1:c.2441A>G
|
XP_011541709.1:p.His814Arg
|
|
XM_011543408.1:c.2720A>G
|
XP_011541710.1:p.His907Arg
|
|
XM_017009484.1:c.2309A>G
|
XP_016864973.1:p.His770Arg
|
|
XM_017009485.1:c.2231A>G
|
XP_016864974.1:p.His744Arg
|
|
XR_001742068.2:n.2751A>G
|
|
|
NM_005921.2:c.2720A>G
MANE Select
|
NP_005912.1:p.His907Arg
|
|