ENST00000338641.10:c.*576G=
MANE Select
|
ENSP00000344666.5:n.*576G=
|
|
ENST00000672461.1:c.*501+135G=
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ENSP00000500919.1:n.*501+135G=
|
|
ENST00000672896.1:c.*636G=
|
ENSP00000500117.1:n.*636G=
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|
ENST00000338641.8:c.*576G=
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ENSP00000344666.4:n.*576G=
|
|
ENST00000361452.8:c.*636G=
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ENSP00000354897.4:n.*636G=
|
|
ENST00000413209.6:c.*576G=
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ENSP00000409921.2:n.*576G=
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|
NM_000268.3:c.*576G= , LRG_511t1:c.*576G=
|
NP_000259.1:n.*576G=
|
|
NM_016418.5:c.*636G= , LRG_511t2:c.*636G=
|
NP_057502.2:n.*636G=
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|
NM_181828.2:c.*636G=
|
NP_861966.1:n.*636G=
|
|
NM_181829.2:c.*636G=
|
NP_861967.1:n.*636G=
|
|
NM_181830.2:c.*636G=
|
NP_861968.1:n.*636G=
|
|
NM_181832.2:c.*651G=
|
NP_861970.1:n.*651G=
|
|
NM_181833.2:c.*576G=
|
NP_861971.1:n.*576G=
|
|
NR_156186.1:n.2923G=
|
|
|
XM_017028810.1:c.*636G=
|
XP_016884299.1:n.*636G=
|
|
NM_000268.4:c.*576G=
MANE Select
|
NP_000259.1:n.*576G=
|
|
NM_181828.3:c.*636G=
|
NP_861966.1:n.*636G=
|
|
NM_181829.3:c.*636G=
|
NP_861967.1:n.*636G=
|
|
NM_181830.3:c.*636G=
|
NP_861968.1:n.*636G=
|
|
NM_181832.3:c.*651G=
|
NP_861970.1:n.*651G=
|
|
NR_156186.2:n.2846G=
|
|
|
NM_181833.3:c.*576G=
|
NP_861971.1:n.*576G=
|
|