ENST00000265512.12:c.978T>C
MANE Select
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ENSP00000265512.7:p.Gly326=
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ENST00000265512.11:c.978T>C
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ENSP00000265512.7:p.Gly326=
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|
ENST00000505590.5:c.1035T>C
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ENSP00000425416.1:p.Gly345=
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ENST00000506705.5:c.*952T>C
|
ENSP00000426667.1:n.*952T>C
|
|
ENST00000508393.5:c.1035T>C
|
ENSP00000424630.1:p.Gly345=
|
|
ENST00000509471.5:c.334-478T>C
|
ENSP00000424583.1:n.334-478T>C
|
|
ENST00000629236.2:c.978T>C
|
ENSP00000486450.1:p.Gly326=
|
|
NM_000670.3:c.978T>C
|
NP_000661.2:p.Gly326=
|
|
NM_000670.4:c.978T>C
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NP_000661.2:p.Gly326=
|
|
NM_001306171.1:c.1035T>C
|
NP_001293100.1:p.Gly345=
|
|
NM_001306172.1:c.1035T>C
|
NP_001293101.1:p.Gly345=
|
|
NR_037884.1:n.429-6345A>G
|
|
|
XR_938685.1:n.1206T>C
|
|
|
XR_938686.1:n.1197T>C
|
|
|
XR_938687.1:n.1070T>C
|
|
|
NM_000670.5:c.978T>C
MANE Select
|
NP_000661.2:p.Gly326=
|
|
NM_001306171.2:c.1035T>C
|
NP_001293100.1:p.Gly345=
|
|
NM_001306172.2:c.1035T>C
|
NP_001293101.1:p.Gly345=
|
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