ENST00000265104.5:c.9412A>C
MANE Select
|
ENSP00000265104.4:p.Ser3138Arg
|
|
ENST00000681290.1:c.9367A>C
|
ENSP00000505288.1:p.Ser3123Arg
|
|
ENST00000265104.4:c.9412A>C
|
ENSP00000265104.4:p.Ser3138Arg
|
|
ENST00000504001.3:n.124A>C
|
|
|
NM_001369.2:c.9412A>C
|
NP_001360.1:p.Ser3138Arg
|
|
XM_005248262.2:c.9367A>C
|
XP_005248319.1:p.Ser3123Arg
|
|
XM_005248262.3:c.9520A>C
|
XP_005248319.2:p.Ser3174Arg
|
|
XM_017009177.1:c.9520A>C
|
XP_016864666.1:p.Ser3174Arg
|
|
XM_017009178.1:c.8425A>C
|
XP_016864667.1:p.Ser2809Arg
|
|
XM_017009179.2:c.8425A>C
|
XP_016864668.1:p.Ser2809Arg
|
|
XM_017009180.1:c.9520A>C
|
XP_016864669.1:p.Ser3174Arg
|
|
XM_017009181.1:c.9520A>C
|
XP_016864670.1:p.Ser3174Arg
|
|
XM_017009182.1:c.9520A>C
|
XP_016864671.1:p.Ser3174Arg
|
|
XM_017009183.1:c.9520A>C
|
XP_016864672.1:p.Ser3174Arg
|
|
XM_017009185.1:c.4609A>C
|
XP_016864674.1:p.Ser1537Arg
|
|
XM_017009186.1:c.4162A>C
|
XP_016864675.1:p.Ser1388Arg
|
|
XM_017009188.1:c.3499A>C
|
XP_016864677.1:p.Ser1167Arg
|
|
XM_024454388.1:c.8425A>C
|
XP_024310156.1:p.Ser2809Arg
|
|
XM_024454389.1:c.8014A>C
|
XP_024310157.1:p.Ser2672Arg
|
|
NM_001369.3:c.9412A>C
MANE Select
|
NP_001360.1:p.Ser3138Arg
|
|