ENST00000029410.10:c.362G>A
MANE Select
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ENSP00000029410.5:p.Arg121Lys
|
|
ENST00000029410.9:c.362G>A
|
ENSP00000029410.5:p.Arg121Lys
|
|
ENST00000502420.1:n.341G>A
|
|
|
ENST00000505433.5:c.362G>A
|
ENSP00000425591.1:p.Arg121Lys
|
|
ENST00000505468.1:c.20G>A
|
ENSP00000420886.1:p.Arg7Lys
|
|
ENST00000507061.1:c.179G>A
|
ENSP00000423868.1:p.Arg60Lys
|
|
ENST00000510761.1:c.20G>A
|
ENSP00000423438.1:p.Arg7Lys
|
|
NM_007255.2:c.362G>A
|
NP_009186.1:p.Arg121Lys
|
|
XM_005265805.2:c.20G>A
|
XP_005265862.1:p.Arg7Lys
|
|
XM_006714816.2:c.-138G>A
|
XP_006714879.1:n.-138G>A
|
|
XM_011534421.1:c.20G>A
|
XP_011532723.1:p.Arg7Lys
|
|
XM_006714816.4:c.-138G>A
|
XP_006714879.1:n.-138G>A
|
|
XM_017008999.2:c.20G>A
|
XP_016864488.1:p.Arg7Lys
|
|
NM_007255.3:c.362G>A
MANE Select
|
NP_009186.1:p.Arg121Lys
|
|