ENST00000682306.1:c.993A>G
MANE Select
|
ENSP00000507664.1:p.Ala331=
|
|
ENST00000323456.9:c.951A>G
|
ENSP00000325285.5:p.Ala317=
|
|
ENST00000579925.5:c.951A>G
|
ENSP00000464067.1:p.Ala317=
|
|
NM_004687.4:c.951A>G
|
NP_004678.3:p.Ala317=
|
|
XM_005257784.2:c.993A>G
|
XP_005257841.1:p.Ala331=
|
|
XM_005257785.3:c.963A>G
|
XP_005257842.1:p.Ala321=
|
|
XM_005257786.3:c.951A>G
|
XP_005257843.1:p.Ala317=
|
|
XM_006722168.2:c.951A>G
|
XP_006722231.1:p.Ala317=
|
|
XM_011525460.1:c.963A>G
|
XP_011523762.1:p.Ala321=
|
|
XM_005257785.5:c.963A>G
|
XP_005257842.1:p.Ala321=
|
|
XM_005257786.5:c.951A>G
|
XP_005257843.1:p.Ala317=
|
|
XM_006722168.4:c.951A>G
|
XP_006722231.1:p.Ala317=
|
|
XM_011525460.3:c.963A>G
|
XP_011523762.1:p.Ala321=
|
|
NM_004687.5:c.951A>G
|
NP_004678.3:p.Ala317=
|
|
NM_001378066.1:c.963A>G
|
NP_001364995.1:p.Ala321=
|
|
NM_001378067.1:c.993A>G
MANE Select
|
NP_001364996.1:p.Ala331=
|
|