ENST00000318471.5:c.564A>T
MANE Select
|
ENSP00000315680.3:p.Ala188=
|
|
ENST00000541292.6:c.564A>T
|
ENSP00000441004.1:p.Ala188=
|
|
ENST00000678002.1:c.252A>T
|
|
|
ENST00000678557.1:c.450A>T
|
ENSP00000502962.1:p.Ala150=
|
|
ENST00000678593.1:c.569A>T
|
ENSP00000503841.1:n.569A>T
|
|
ENST00000679286.1:c.444A>T
|
ENSP00000503168.1:p.Ala148=
|
|
ENST00000318471.4:c.564A>T
|
ENSP00000315680.3:p.Ala188=
|
|
ENST00000541292.5:c.564A>T
|
ENSP00000441004.1:p.Ala188=
|
|
NM_000288.3:c.564A>T
|
NP_000279.1:p.Ala188=
|
|
XM_005267019.3:c.450A>T
|
XP_005267076.1:p.Ala150=
|
|
XM_006715502.1:c.340-3226A>T
|
XP_006715565.1:n.340-3226A>T
|
|
XM_011535900.1:c.526+20483A>T
|
XP_011534202.1:n.526+20483A>T
|
|
XM_005267019.4:c.450A>T
|
XP_005267076.1:p.Ala150=
|
|
XM_006715502.2:c.340-3226A>T
|
XP_006715565.1:n.340-3226A>T
|
|
XM_017010934.2:c.526+20483A>T
|
XP_016866423.1:n.526+20483A>T
|
|
NM_000288.4:c.564A>T
MANE Select
|
NP_000279.1:p.Ala188=
|
|