ENST00000375128.5:c.780T>G
MANE Select
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ENSP00000364270.5:p.Thr260=
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ENST00000375128.4:c.780T>G
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ENSP00000364270.4:p.Thr260=
|
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ENST00000462523.5:c.*216T>G
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ENSP00000433006.1:n.*216T>G
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ENST00000485042.1:n.292T>G
|
|
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NM_000380.3:c.780T>G , LRG_471t1:c.780T>G
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NP_000371.1:p.Thr260=
|
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NR_027302.1:n.1128T>G
|
|
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XM_006717278.1:c.772+8T>G
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XP_006717341.1:n.772+8T>G
|
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XM_011518988.1:c.772+8T>G
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XP_011517290.1:n.772+8T>G
|
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NM_001354975.1:c.654T>G
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NP_001341904.1:p.Thr218=
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NR_149091.1:n.625T>G
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|
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NR_149092.1:n.791T>G
|
|
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NR_149093.1:n.1317T>G
|
|
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NR_149094.1:n.1211T>G
|
|
|
NM_000380.4:c.780T>G
MANE Select
|
NP_000371.1:p.Thr260=
|
|
NM_001354975.2:c.654T>G
|
NP_001341904.1:p.Thr218=
|
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NR_027302.2:n.1059T>G
|
|
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NR_149091.2:n.556T>G
|
|
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NR_149092.2:n.722T>G
|
|
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NR_149093.2:n.1248T>G
|
|
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NR_149094.2:n.1142T>G
|
|
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