ENST00000356392.9:c.922G>T
MANE Select
|
ENSP00000348757.3:p.Ala308Ser
|
|
ENST00000356392.8:c.922G>T
|
ENSP00000348757.3:p.Ala308Ser
|
|
ENST00000586836.5:c.349G>T
|
ENSP00000467429.1:p.Ala117Ser
|
|
ENST00000591179.5:c.742G>T
|
ENSP00000466800.1:p.Ala248Ser
|
|
ENST00000591345.5:c.*841G>T
|
ENSP00000467313.1:n.*841G>T
|
|
NM_001302453.1:c.760G>T
|
NP_001289382.1:p.Ala254Ser
|
|
NM_001302454.1:c.742G>T
|
NP_001289383.1:p.Ala248Ser
|
|
NM_145045.4:c.922G>T
|
NP_659482.3:p.Ala308Ser
|
|
XM_017026241.1:c.904+18G>T
|
XP_016881730.1:n.904+18G>T
|
|
NM_145045.5:c.922G>T
MANE Select
|
NP_659482.3:p.Ala308Ser
|
|
NM_001302454.2:c.742G>T
|
NP_001289383.1:p.Ala248Ser
|
|