ENST00000696156.1:c.479T=
|
ENSP00000512446.1:p.Ile160=
|
|
ENST00000696157.1:c.*780T=
|
ENSP00000512447.1:n.*780T=
|
|
ENST00000696158.1:c.*817T=
|
ENSP00000512448.1:n.*817T=
|
|
ENST00000696159.1:c.*486T=
|
ENSP00000512449.1:n.*486T=
|
|
ENST00000696160.1:c.590T=
|
ENSP00000512450.1:p.Ile197=
|
|
ENST00000696161.1:c.693T=
|
ENSP00000512451.1:p.His231=
|
|
ENST00000696162.1:c.*1282T=
|
ENSP00000512452.1:n.*1282T=
|
|
ENST00000696163.1:c.512T=
|
ENSP00000512453.1:p.Ile171=
|
|
ENST00000261623.8:c.563T=
MANE Select
|
ENSP00000261623.3:p.Ile188=
|
|
ENST00000261623.7:c.563T=
|
ENSP00000261623.3:p.Ile188=
|
|
NM_000101.3:c.563T=
|
NP_000092.2:p.Ile188=
|
|
NM_000101.4:c.563T=
MANE Select
|
NP_000092.2:p.Ile188=
|
|