ENST00000367435.5:c.1017A>C
MANE Select
|
ENSP00000356405.4:p.Pro339=
|
|
ENST00000635846.1:c.774A>C
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ENSP00000490035.1:p.Pro258=
|
|
ENST00000643006.1:c.1085A>C
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ENSP00000496633.1:p.Gln362Pro
|
|
ENST00000648071.1:c.*993A>C
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ENSP00000497513.1:n.*993A>C
|
|
ENST00000649613.1:n.267A>C
|
|
|
ENST00000649895.1:n.1235A>C
|
|
|
ENST00000650197.1:c.1017A>C
|
ENSP00000496929.1:p.Pro339=
|
|
ENST00000367435.3:c.1017A>C
|
ENSP00000356405.3:p.Pro339=
|
|
NM_024529.4:c.1017A>C , LRG_507t1:c.1017A>C
|
NP_078805.3:p.Pro339=
|
|
NM_024529.5:c.1017A>C
MANE Select
|
NP_078805.3:p.Pro339=
|
|