ENST00000366159.9:n.2115T=
|
|
|
ENST00000437813.8:c.*475T=
|
ENSP00000513672.1:n.*475T=
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|
ENST00000440083.7:c.1233T=
|
ENSP00000413224.3:p.Leu411=
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|
ENST00000535958.2:c.*841T=
|
ENSP00000513673.1:n.*841T=
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|
ENST00000698337.1:n.975T=
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|
|
ENST00000698338.1:n.1628T=
|
|
|
ENST00000698339.1:c.*509T=
|
ENSP00000513670.1:n.*509T=
|
|
ENST00000698340.1:c.*253T=
|
ENSP00000513671.1:n.*253T=
|
|
ENST00000162749.7:c.1014T=
MANE Select
|
ENSP00000162749.2:p.Leu338=
|
|
ENST00000162749.6:c.1014T=
|
ENSP00000162749.2:p.Leu338=
|
|
ENST00000534885.5:c.*491T=
|
ENSP00000441803.1:n.*491T=
|
|
ENST00000536717.5:n.918T=
|
|
|
ENST00000540022.5:c.885T=
|
ENSP00000438343.1:p.Leu295=
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|
ENST00000543359.5:n.426T=
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|
|
ENST00000543995.5:c.*601T=
|
ENSP00000442405.1:n.*601T=
|
|
NM_001065.3:c.1014T= , LRG_193t1:c.1014T=
|
NP_001056.1:p.Leu338=
|
|
NM_001346091.1:c.690T=
|
NP_001333020.1:p.Leu230=
|
|
NM_001346092.1:c.555T=
|
NP_001333021.1:p.Leu185=
|
|
NR_144351.1:n.1243T=
|
|
|
NM_001065.4:c.1014T=
MANE Select
|
NP_001056.1:p.Leu338=
|
|
NM_001346091.2:c.690T=
|
NP_001333020.1:p.Leu230=
|
|
NM_001346092.2:c.555T=
|
NP_001333021.1:p.Leu185=
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|
NR_144351.2:n.1202T=
|
|
|