ENST00000270301.12:c.4155A>T
|
ENSP00000270301.6:p.Leu1385Phe
|
|
ENST00000401500.7:c.4170A>T
MANE Select
|
ENSP00000384792.1:p.Leu1390Phe
|
|
ENST00000587391.6:c.*4030A>T
|
ENSP00000465525.1:n.*4030A>T
|
|
ENST00000679357.1:c.2250A>T
|
|
|
ENST00000679598.1:c.919-4A>T
|
|
|
ENST00000679682.1:c.4155A>T
|
ENSP00000506226.1:p.Leu1385Phe
|
|
ENST00000679714.1:c.4164A>T
|
ENSP00000506627.1:p.Leu1388Phe
|
|
ENST00000679757.1:c.3819A>T
|
ENSP00000505158.1:p.Leu1273Phe
|
|
ENST00000679858.1:c.*3552A>T
|
ENSP00000505655.1:n.*3552A>T
|
|
ENST00000680211.1:c.771A>T
|
ENSP00000506102.1:p.Leu257Phe
|
|
ENST00000680280.1:n.1673A>T
|
|
|
ENST00000680349.1:n.2819A>T
|
|
|
ENST00000680403.1:c.4155A>T
|
ENSP00000505677.1:p.Leu1385Phe
|
|
ENST00000680564.1:c.3921A>T
|
ENSP00000505582.1:p.Leu1307Phe
|
|
ENST00000680590.1:c.*2550A>T
|
ENSP00000505350.1:n.*2550A>T
|
|
ENST00000680597.1:c.903A>T
|
|
|
ENST00000680739.1:c.1185A>T
|
|
|
ENST00000680773.1:n.2671A>T
|
|
|
ENST00000680806.1:c.*3473A>T
|
ENSP00000506418.1:n.*3473A>T
|
|
ENST00000680997.1:n.2102A>T
|
|
|
ENST00000681608.1:n.2015A>T
|
|
|
ENST00000681625.1:c.*1502A>T
|
ENSP00000505555.1:n.*1502A>T
|
|
ENST00000681648.1:n.2221A>T
|
|
|
ENST00000270301.11:c.4155A>T
|
ENSP00000270301.6:p.Leu1385Phe
|
|
ENST00000401500.6:c.4170A>T
|
ENSP00000384792.1:p.Leu1390Phe
|
|
ENST00000587391.5:c.*4030A>T
|
ENSP00000465525.1:n.*4030A>T
|
|
NM_001083961.1:c.4170A>T
|
NP_001077430.1:p.Leu1390Phe
|
|
NM_173636.4:c.4155A>T
|
NP_775907.4:p.Leu1385Phe
|
|
XM_005258809.2:c.4059A>T
|
XP_005258866.1:p.Leu1353Phe
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|
XM_011526837.1:c.4155A>T
|
XP_011525139.1:p.Leu1385Phe
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|
XM_011526838.1:c.3921A>T
|
XP_011525140.1:p.Leu1307Phe
|
|
XM_011526839.1:c.3819A>T
|
XP_011525141.1:p.Leu1273Phe
|
|
XM_011526840.1:c.3162A>T
|
XP_011525142.1:p.Leu1054Phe
|
|
XM_011526841.1:c.2748A>T
|
XP_011525143.1:p.Leu916Phe
|
|
XM_011526842.1:c.2601A>T
|
XP_011525144.1:p.Leu867Phe
|
|
XM_011526843.1:c.1917A>T
|
XP_011525145.1:p.Leu639Phe
|
|
XM_011526844.1:c.1917A>T
|
XP_011525146.1:p.Leu639Phe
|
|
XM_011526840.2:c.3162A>T
|
XP_011525142.1:p.Leu1054Phe
|
|
XM_011526841.2:c.2748A>T
|
XP_011525143.1:p.Leu916Phe
|
|
XM_011526844.2:c.1917A>T
|
XP_011525146.1:p.Leu639Phe
|
|
XM_017026665.1:c.4170A>T
|
XP_016882154.1:p.Leu1390Phe
|
|
NM_001083961.2:c.4170A>T
MANE Select
|
NP_001077430.1:p.Leu1390Phe
|
|
NM_173636.5:c.4155A>T
|
NP_775907.4:p.Leu1385Phe
|
|