ENST00000399503.4:c.2640A>G
MANE Select
|
ENSP00000382423.3:p.Gln880=
|
|
ENST00000399503.3:c.2640A>G
|
ENSP00000382423.3:p.Gln880=
|
|
NM_005921.1:c.2640A>G
|
NP_005912.1:p.Gln880=
|
|
XM_005248519.3:c.2262A>G
|
XP_005248576.2:p.Gln754=
|
|
XM_011543406.1:c.2385A>G
|
XP_011541708.1:p.Gln795=
|
|
XM_011543407.1:c.2361A>G
|
XP_011541709.1:p.Gln787=
|
|
XM_011543408.1:c.2640A>G
|
XP_011541710.1:p.Gln880=
|
|
XM_017009484.1:c.2229A>G
|
XP_016864973.1:p.Gln743=
|
|
XM_017009485.1:c.2151A>G
|
XP_016864974.1:p.Gln717=
|
|
XR_001742068.2:n.2671A>G
|
|
|
NM_005921.2:c.2640A>G
MANE Select
|
NP_005912.1:p.Gln880=
|
|