ENST00000526008.6:c.*2073G=
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ENSP00000513006.1:n.*2073G=
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|
ENST00000696967.1:n.2693G=
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|
|
ENST00000696968.1:n.749G=
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|
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ENST00000696969.1:n.2473G=
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|
|
ENST00000458235.7:c.*141G=
MANE Select
|
ENSP00000391676.1:n.*141G=
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ENST00000458235.5:c.*141G=
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ENSP00000391676.1:n.*141G=
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ENST00000527031.5:n.2279-1292G=
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|
|
ENST00000527670.5:c.*141G=
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ENSP00000432511.1:n.*141G=
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|
NM_000215.3:c.*141G= , LRG_77t1:c.*141G=
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NP_000206.2:n.*141G=
|
|
XM_005259896.2:c.*141G=
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XP_005259953.1:n.*141G=
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|
XM_006722745.2:c.*141G=
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XP_006722808.1:n.*141G=
|
|
XM_005259896.3:c.*141G=
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XP_005259953.1:n.*141G=
|
|
NM_000215.4:c.*141G=
MANE Select
|
NP_000206.2:n.*141G=
|
|