ENST00000325385.12:c.2011A>G
MANE Select
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ENSP00000315569.7:p.Met671Val
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ENST00000273009.10:c.1582-9505A>G
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ENSP00000273009.6:n.1582-9505A>G
|
|
ENST00000325385.11:c.2011A>G
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ENSP00000315569.7:p.Met671Val
|
|
ENST00000390005.9:c.*78A>G
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ENSP00000374655.5:n.*78A>G
|
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ENST00000409307.5:c.2011A>G
|
ENSP00000386799.1:p.Met671Val
|
|
ENST00000424049.1:c.916A>G
|
ENSP00000415419.1:p.Met306Val
|
|
ENST00000429283.2:n.1577A>G
|
|
|
ENST00000433430.5:c.3422A>G
|
ENSP00000391175.1:n.3422A>G
|
|
ENST00000445090.5:c.*1167A>G
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ENSP00000388999.1:n.*1167A>G
|
|
NM_001257281.1:c.1582-9505A>G
|
NP_001244210.1:n.1582-9505A>G
|
|
NM_152383.4:c.2011A>G , LRG_534t1:c.2011A>G
|
NP_689596.4:p.Met671Val
|
|
NR_046476.1:n.2214A>G
|
|
|
NR_046477.1:n.2193A>G
|
|
|
NM_001257281.2:c.1582-9505A>G
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NP_001244210.1:n.1582-9505A>G
|
|
NM_152383.5:c.2011A>G
MANE Select
|
NP_689596.4:p.Met671Val
|
|
NR_046476.2:n.2084A>G
|
|
|
NR_046477.2:n.2063A>G
|
|
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