ENST00000480188.2:n.923G=
|
|
|
ENST00000696279.1:c.4332G=
|
|
|
ENST00000696280.1:n.4101G=
|
|
|
ENST00000696281.1:c.4030G=
|
ENSP00000512521.1:p.Val1344=
|
|
ENST00000697921.1:n.2890G=
|
|
|
ENST00000697922.1:c.*4002G=
|
ENSP00000513478.1:n.*4002G=
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|
ENST00000697923.1:n.4457G=
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|
|
ENST00000223642.3:c.4012G=
MANE Select
|
ENSP00000223642.1:p.Val1338=
|
|
ENST00000223642.2:c.4012G=
|
ENSP00000223642.1:p.Val1338=
|
|
NM_001735.2:c.4012G= , LRG_28t1:c.4012G=
|
NP_001726.2:p.Val1338=
|
|
XM_011518980.1:c.4027G=
|
XP_011517282.1:p.Val1343=
|
|
NM_001317163.1:c.4030G=
|
NP_001304092.1:p.Val1344=
|
|
NM_001317163.2:c.4030G=
|
NP_001304092.1:p.Val1344=
|
|
NM_001735.3:c.4012G=
MANE Select
|
NP_001726.2:p.Val1338=
|
|