ENST00000264028.5:c.1530T>C
MANE Select
|
ENSP00000264028.4:p.Ile510=
|
|
ENST00000264028.4:c.1530T>C
|
ENSP00000264028.4:p.Ile510=
|
|
ENST00000359415.8:c.1653T>C
|
ENSP00000352385.4:p.Ile551=
|
|
ENST00000392859.7:c.1266T>C
|
ENSP00000376599.3:p.Ile422=
|
|
ENST00000534182.2:c.160-928T>C
|
ENSP00000431676.1:n.160-928T>C
|
|
ENST00000614498.4:c.509-614T>C
|
ENSP00000482114.1:n.509-614T>C
|
|
NM_001142281.1:c.1266T>C
|
NP_001135753.1:p.Ile422=
|
|
NM_001655.4:c.1530T>C
|
NP_001646.2:p.Ile510=
|
|
XM_005271542.2:c.*71T>C
|
XP_005271599.1:n.*71T>C
|
|
XM_005271542.4:c.*71T>C
|
XP_005271599.1:n.*71T>C
|
|
NM_001655.5:c.1530T>C
MANE Select
|
NP_001646.2:p.Ile510=
|
|
NM_001142281.2:c.1266T>C
|
NP_001135753.1:p.Ile422=
|
|