ENST00000265512.12:c.892A=
MANE Select
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ENSP00000265512.7:p.Ile298=
|
|
ENST00000265512.11:c.892A=
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ENSP00000265512.7:p.Ile298=
|
|
ENST00000505590.5:c.949A=
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ENSP00000425416.1:p.Ile317=
|
|
ENST00000506705.5:c.*866A=
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ENSP00000426667.1:n.*866A=
|
|
ENST00000508393.5:c.949A=
|
ENSP00000424630.1:p.Ile317=
|
|
ENST00000509471.5:c.334-564A=
|
ENSP00000424583.1:n.334-564A=
|
|
ENST00000629236.2:c.892A=
|
ENSP00000486450.1:p.Ile298=
|
|
NM_000670.3:c.892A=
|
NP_000661.2:p.Ile298=
|
|
NM_000670.4:c.892A=
|
NP_000661.2:p.Ile298=
|
|
NM_001306171.1:c.949A=
|
NP_001293100.1:p.Ile317=
|
|
NM_001306172.1:c.949A=
|
NP_001293101.1:p.Ile317=
|
|
NR_037884.1:n.429-6259T=
|
|
|
XR_938685.1:n.1120A=
|
|
|
XR_938686.1:n.1111A=
|
|
|
XR_938687.1:n.984A=
|
|
|
NM_000670.5:c.892A=
MANE Select
|
NP_000661.2:p.Ile298=
|
|
NM_001306171.2:c.949A=
|
NP_001293100.1:p.Ile317=
|
|
NM_001306172.2:c.949A=
|
NP_001293101.1:p.Ile317=
|
|