ENST00000371746.9:c.984C>T
|
ENSP00000360811.3:p.Ala328=
|
|
ENST00000371748.10:c.969C>T
MANE Select
|
ENSP00000360813.4:p.Ala323=
|
|
ENST00000645419.1:n.1794C>T
|
|
|
ENST00000371746.7:c.984C>T
|
ENSP00000360811.3:p.Ala328=
|
|
ENST00000371748.9:c.969C>T
|
ENSP00000360813.4:p.Ala323=
|
|
ENST00000619587.1:c.936C>T
|
ENSP00000483080.1:p.Ala312=
|
|
NM_014564.3:c.984C>T
|
NP_055379.1:p.Ala328=
|
|
NM_178138.4:c.969C>T
|
NP_835258.1:p.Ala323=
|
|
XM_005263410.1:c.936C>T
|
XP_005263467.1:p.Ala312=
|
|
NM_001363746.1:c.936C>T
|
NP_001350675.1:p.Ala312=
|
|
NM_014564.4:c.984C>T
|
NP_055379.1:p.Ala328=
|
|
NM_178138.5:c.969C>T
|
NP_835258.1:p.Ala323=
|
|
XM_017015168.1:c.897C>T
|
XP_016870657.1:p.Ala299=
|
|
NM_178138.6:c.969C>T
MANE Select
|
NP_835258.1:p.Ala323=
|
|
NM_014564.5:c.984C>T
|
NP_055379.1:p.Ala328=
|
|