ENST00000366835.8:c.1804G>T
MANE Select
|
ENSP00000355800.3:p.Ala602Ser
|
|
ENST00000366835.7:c.1804G>T
|
ENSP00000355800.3:p.Ala602Ser
|
|
NM_014698.2:c.1804G>T
|
NP_055513.2:p.Ala602Ser
|
|
XM_006711841.2:c.1273G>T
|
XP_006711904.1:p.Ala425Ser
|
|
XM_011544328.1:c.1804G>T
|
XP_011542630.1:p.Ala602Ser
|
|
XM_011544329.1:c.1804G>T
|
XP_011542631.1:p.Ala602Ser
|
|
XM_011544330.1:c.1804G>T
|
XP_011542632.1:p.Ala602Ser
|
|
XM_011544331.1:c.1717G>T
|
XP_011542633.1:p.Ala573Ser
|
|
XM_011544332.1:c.1363G>T
|
XP_011542634.1:p.Ala455Ser
|
|
XR_949163.1:n.2109G>T
|
|
|
XM_006711841.4:c.1273G>T
|
XP_006711904.1:p.Ala425Ser
|
|
XM_011544328.3:c.1804G>T
|
XP_011542630.1:p.Ala602Ser
|
|
XM_011544329.3:c.1804G>T
|
XP_011542631.1:p.Ala602Ser
|
|
XM_011544330.3:c.1804G>T
|
XP_011542632.1:p.Ala602Ser
|
|
XM_011544331.3:c.1717G>T
|
XP_011542633.1:p.Ala573Ser
|
|
XM_011544332.3:c.1363G>T
|
XP_011542634.1:p.Ala455Ser
|
|
XR_001737552.2:n.1891G>T
|
|
|
XR_949163.3:n.2088G>T
|
|
|
NM_014698.3:c.1804G>T
MANE Select
|
NP_055513.2:p.Ala602Ser
|
|