ENST00000278853.10:c.1598C>T
MANE Select
|
ENSP00000278853.5:p.Ala533Val
|
|
ENST00000278853.9:c.1598C>T
|
ENSP00000278853.5:p.Ala533Val
|
|
ENST00000537203.5:n.1217C>T
|
|
|
ENST00000543020.1:n.523C>T
|
|
|
ENST00000620319.1:c.719C>T
|
ENSP00000480463.1:p.Ala240Val
|
|
NM_207341.3:c.1598C>T
|
NP_997224.2:p.Ala533Val
|
|
XM_011544852.1:c.719C>T
|
XP_011543154.1:p.Ala240Val
|
|
XM_011544853.1:c.719C>T
|
XP_011543155.1:p.Ala240Val
|
|
XM_011544852.2:c.719C>T
|
XP_011543154.1:p.Ala240Val
|
|
XM_011544853.2:c.719C>T
|
XP_011543155.1:p.Ala240Val
|
|
NM_001391943.1:c.719C>T
|
NP_001378872.1:p.Ala240Val
|
|
NM_001391944.1:c.404C>T
|
NP_001378873.1:p.Ala135Val
|
|
NM_207341.4:c.1598C>T
MANE Select
|
NP_997224.2:p.Ala533Val
|
|