ENST00000256996.9:c.978G>C
MANE Select
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ENSP00000256996.4:p.Leu326=
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ENST00000256996.8:c.978G>C
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ENSP00000256996.3:p.Leu326=
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ENST00000378600.7:c.457-2470G>C
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ENSP00000367863.3:n.457-2470G>C
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ENST00000378601.7:c.*65G>C
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ENSP00000367864.3:n.*65G>C
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ENST00000378603.7:c.786G>C
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ENSP00000367866.3:p.Leu262=
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ENST00000612309.4:n.2427G>C
|
|
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ENST00000614394.1:n.368G>C
|
|
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ENST00000616278.4:c.654G>C
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ENSP00000478411.1:n.654G>C
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ENST00000617022.4:n.1554-2470G>C
|
|
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ENST00000617847.4:c.907G>C
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|
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ENST00000620515.1:n.144G>C
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|
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NM_000107.2:c.978G>C , LRG_467t1:c.978G>C
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NP_000098.1:p.Leu326=
|
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NM_001300734.1:c.457-2470G>C
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NP_001287663.1:n.457-2470G>C
|
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XR_242780.3:n.968G>C
|
|
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XR_242780.4:n.968G>C
|
|
|
NM_000107.3:c.978G>C
MANE Select
|
NP_000098.1:p.Leu326=
|
|
NM_001300734.2:c.457-2470G>C
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NP_001287663.1:n.457-2470G>C
|
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NM_001399874.1:c.978G>C
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NP_001386803.1:p.Leu326=
|
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NM_001399875.1:c.978G>C
|
NP_001386804.1:p.Leu326=
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|
NM_001399876.1:c.457-2470G>C
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NP_001386805.1:n.457-2470G>C
|
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NM_001399878.1:c.786G>C
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NP_001386807.1:p.Leu262=
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NR_174610.1:n.1229G>C
|
|
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NR_174611.1:n.1207G>C
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