ENST00000371270.6:c.1413A=
MANE Select
|
ENSP00000360317.3:p.Ala471=
|
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ENST00000371270.5:c.1413A=
|
ENSP00000360317.3:p.Ala471=
|
|
ENST00000490994.6:c.*1199A=
|
ENSP00000433314.1:n.*1199A=
|
|
ENST00000525991.5:c.*988A=
|
ENSP00000433842.1:n.*988A=
|
|
ENST00000526814.5:n.1668A=
|
|
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ENST00000527420.5:c.*270A=
|
ENSP00000433191.1:n.*270A=
|
|
ENST00000527953.5:n.1707A=
|
|
|
ENST00000531714.1:n.601A=
|
|
|
ENST00000533320.5:n.1647A=
|
|
|
ENST00000535898.5:c.1107A=
|
ENSP00000445062.1:p.Ala369=
|
|
ENST00000539050.5:c.1203A=
|
ENSP00000442343.2:p.Ala401=
|
|
ENST00000623108.3:c.1203A=
|
ENSP00000485110.1:p.Ala401=
|
|
NM_000770.3:c.1413A=
MANE Select
|
NP_000761.3:p.Ala471=
|
|
NM_001198853.1:c.1203A=
|
NP_001185782.1:p.Ala401=
|
|
NM_001198854.1:c.1107A=
|
NP_001185783.1:p.Ala369=
|
|
NM_001198855.1:c.1203A=
|
NP_001185784.1:p.Ala401=
|
|
XR_945610.1:n.1548A=
|
|
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