ENST00000383168.9:c.*1042G=
MANE Select
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ENSP00000372654.4:n.*1042G=
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|
ENST00000672188.1:c.*1042G=
|
ENSP00000500720.1:n.*1042G=
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|
ENST00000672981.2:c.*955G=
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ENSP00000500598.2:n.*955G=
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|
ENST00000383168.8:c.*1042G=
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ENSP00000372654.4:n.*1042G=
|
|
NM_001650.4:c.*1042G=
|
NP_001641.1:n.*1042G=
|
|
NM_004028.3:c.*1042G=
|
NP_004019.1:n.*1042G=
|
|
XM_011525942.1:c.*1042G=
|
XP_011524244.1:n.*1042G=
|
|
NM_001317384.2:c.*955G=
|
NP_001304313.1:n.*955G=
|
|
NM_001317387.2:c.*1042G=
|
NP_001304316.1:n.*1042G=
|
|
NM_001364286.1:c.*1042G=
|
NP_001351215.1:n.*1042G=
|
|
NM_001364287.1:c.*955G=
|
NP_001351216.1:n.*955G=
|
|
NM_001364289.1:c.*955G=
|
NP_001351218.1:n.*955G=
|
|
NM_001650.6:c.*1042G=
|
NP_001641.1:n.*1042G=
|
|
NM_004028.4:c.*1042G=
|
NP_004019.1:n.*1042G=
|
|
XM_011525942.3:c.*1042G=
|
XP_011524244.1:n.*1042G=
|
|
NM_001650.7:c.*1042G=
MANE Select
|
NP_001641.1:n.*1042G=
|
|
NM_001317384.3:c.*955G=
|
NP_001304313.1:n.*955G=
|
|
NM_001317387.3:c.*1042G=
|
NP_001304316.1:n.*1042G=
|
|
NM_001364289.2:c.*955G=
|
NP_001351218.1:n.*955G=
|
|
NM_004028.5:c.*1042G=
|
NP_004019.1:n.*1042G=
|
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