|
ENST00000445061.6:c.2321C>T
MANE Select
|
ENSP00000405620.1:p.Ala774Val
|
|
|
ENST00000348968.8:c.2237C>T
|
ENSP00000343442.4:p.Ala746Val
|
|
|
ENST00000395745.6:c.*2221C>T
|
ENSP00000379094.2:n.*2221C>T
|
|
|
ENST00000445061.5:c.2321C>T
|
ENSP00000405620.1:p.Ala774Val
|
|
|
ENST00000446256.6:c.2321C>T
|
ENSP00000392601.3:p.Ala774Val
|
|
|
ENST00000457607.1:c.2405C>T
|
ENSP00000394682.1:p.Ala802Val
|
|
|
ENST00000474183.1:n.438C>T
|
|
|
|
ENST00000619982.4:c.2204C>T
|
ENSP00000483160.1:p.Ala735Val
|
|
|
NM_014966.3:c.2204C>T
|
NP_055781.2:p.Ala735Val
|
|
|
NM_138615.2:c.2321C>T
|
NP_619520.1:p.Ala774Val
|
|
|
XM_006713033.1:c.2225C>T
|
XP_006713096.1:p.Ala742Val
|
|
|
XM_011533490.1:c.2534C>T
|
XP_011531792.1:p.Ala845Val
|
|
|
XM_011533491.1:c.2534C>T
|
XP_011531793.1:p.Ala845Val
|
|
|
XM_011533492.1:c.2534C>T
|
XP_011531794.1:p.Ala845Val
|
|
|
XM_011533493.1:c.2423C>T
|
XP_011531795.1:p.Ala808Val
|
|
|
XM_011533494.1:c.2321C>T
|
XP_011531796.1:p.Ala774Val
|
|
|
XM_011533495.1:c.2321C>T
|
XP_011531797.1:p.Ala774Val
|
|
|
XM_011533496.1:c.2237C>T
|
XP_011531798.1:p.Ala746Val
|
|
|
XM_011533497.1:c.2237C>T
|
XP_011531799.1:p.Ala746Val
|
|
|
XM_011533498.1:c.2237C>T
|
XP_011531800.1:p.Ala746Val
|
|
|
NM_001330990.1:c.2237C>T
|
NP_001317919.1:p.Ala746Val
|
|
|
XM_011533490.2:c.2534C>T
|
XP_011531792.1:p.Ala845Val
|
|
|
XM_011533494.3:c.2321C>T
|
XP_011531796.1:p.Ala774Val
|
|
|
XM_011533495.2:c.2321C>T
|
XP_011531797.1:p.Ala774Val
|
|
|
XM_011533497.2:c.2237C>T
|
XP_011531799.1:p.Ala746Val
|
|
|
XM_017005914.1:c.2453C>T
|
XP_016861403.1:p.Ala818Val
|
|
|
XM_017005915.1:c.2225C>T
|
XP_016861404.1:p.Ala742Val
|
|
|
XM_017005916.2:c.2210C>T
|
XP_016861405.1:p.Ala737Val
|
|
|
XM_017005917.1:c.2204C>T
|
XP_016861406.1:p.Ala735Val
|
|
|
XM_024453405.1:c.2423C>T
|
XP_024309173.1:p.Ala808Val
|
|
|
NM_138615.3:c.2321C>T
MANE Select
|
NP_619520.1:p.Ala774Val
|
|
|
NM_001330990.2:c.2237C>T
|
NP_001317919.1:p.Ala746Val
|
|
|
NM_014966.4:c.2204C>T
|
NP_055781.2:p.Ala735Val
|
|
