ENST00000371746.9:c.977C>A
|
ENSP00000360811.3:p.Pro326His
|
|
ENST00000371748.10:c.962C>A
MANE Select
|
ENSP00000360813.4:p.Pro321His
|
|
ENST00000645419.1:n.1787C>A
|
|
|
ENST00000371746.7:c.977C>A
|
ENSP00000360811.3:p.Pro326His
|
|
ENST00000371748.9:c.962C>A
|
ENSP00000360813.4:p.Pro321His
|
|
ENST00000619587.1:c.929C>A
|
ENSP00000483080.1:p.Pro310His
|
|
NM_014564.3:c.977C>A
|
NP_055379.1:p.Pro326His
|
|
NM_178138.4:c.962C>A
|
NP_835258.1:p.Pro321His
|
|
XM_005263410.1:c.929C>A
|
XP_005263467.1:p.Pro310His
|
|
NM_001363746.1:c.929C>A
|
NP_001350675.1:p.Pro310His
|
|
NM_014564.4:c.977C>A
|
NP_055379.1:p.Pro326His
|
|
NM_178138.5:c.962C>A
|
NP_835258.1:p.Pro321His
|
|
XM_017015168.1:c.890C>A
|
XP_016870657.1:p.Pro297His
|
|
NM_178138.6:c.962C>A
MANE Select
|
NP_835258.1:p.Pro321His
|
|
NM_014564.5:c.977C>A
|
NP_055379.1:p.Pro326His
|
|