ENST00000270301.12:c.4248G>C
|
ENSP00000270301.6:p.Leu1416Phe
|
|
ENST00000401500.7:c.4263G>C
MANE Select
|
ENSP00000384792.1:p.Leu1421Phe
|
|
ENST00000587391.6:c.*4123G>C
|
ENSP00000465525.1:n.*4123G>C
|
|
ENST00000679357.1:c.2343G>C
|
|
|
ENST00000679598.1:c.1008G>C
|
|
|
ENST00000679682.1:c.4248G>C
|
ENSP00000506226.1:p.Leu1416Phe
|
|
ENST00000679714.1:c.4257G>C
|
ENSP00000506627.1:p.Leu1419Phe
|
|
ENST00000679757.1:c.3912G>C
|
ENSP00000505158.1:p.Leu1304Phe
|
|
ENST00000679858.1:c.*3645G>C
|
ENSP00000505655.1:n.*3645G>C
|
|
ENST00000680211.1:c.864G>C
|
ENSP00000506102.1:p.Leu288Phe
|
|
ENST00000680280.1:n.1766G>C
|
|
|
ENST00000680349.1:n.2912G>C
|
|
|
ENST00000680403.1:c.4248G>C
|
ENSP00000505677.1:p.Leu1416Phe
|
|
ENST00000680564.1:c.4014G>C
|
ENSP00000505582.1:p.Leu1338Phe
|
|
ENST00000680590.1:c.*2643G>C
|
ENSP00000505350.1:n.*2643G>C
|
|
ENST00000680597.1:c.996G>C
|
|
|
ENST00000680739.1:c.1278G>C
|
|
|
ENST00000680773.1:n.2764G>C
|
|
|
ENST00000680806.1:c.*3566G>C
|
ENSP00000506418.1:n.*3566G>C
|
|
ENST00000680997.1:n.2195G>C
|
|
|
ENST00000681608.1:n.2108G>C
|
|
|
ENST00000681625.1:c.*1595G>C
|
ENSP00000505555.1:n.*1595G>C
|
|
ENST00000681648.1:n.2314G>C
|
|
|
ENST00000270301.11:c.4248G>C
|
ENSP00000270301.6:p.Leu1416Phe
|
|
ENST00000401500.6:c.4263G>C
|
ENSP00000384792.1:p.Leu1421Phe
|
|
ENST00000587391.5:c.*4123G>C
|
ENSP00000465525.1:n.*4123G>C
|
|
NM_001083961.1:c.4263G>C
|
NP_001077430.1:p.Leu1421Phe
|
|
NM_173636.4:c.4248G>C
|
NP_775907.4:p.Leu1416Phe
|
|
XM_005258809.2:c.4152G>C
|
XP_005258866.1:p.Leu1384Phe
|
|
XM_011526837.1:c.4248G>C
|
XP_011525139.1:p.Leu1416Phe
|
|
XM_011526838.1:c.4014G>C
|
XP_011525140.1:p.Leu1338Phe
|
|
XM_011526839.1:c.3912G>C
|
XP_011525141.1:p.Leu1304Phe
|
|
XM_011526840.1:c.3255G>C
|
XP_011525142.1:p.Leu1085Phe
|
|
XM_011526841.1:c.2841G>C
|
XP_011525143.1:p.Leu947Phe
|
|
XM_011526842.1:c.2694G>C
|
XP_011525144.1:p.Leu898Phe
|
|
XM_011526843.1:c.2010G>C
|
XP_011525145.1:p.Leu670Phe
|
|
XM_011526844.1:c.2010G>C
|
XP_011525146.1:p.Leu670Phe
|
|
XM_011526840.2:c.3255G>C
|
XP_011525142.1:p.Leu1085Phe
|
|
XM_011526841.2:c.2841G>C
|
XP_011525143.1:p.Leu947Phe
|
|
XM_011526844.2:c.2010G>C
|
XP_011525146.1:p.Leu670Phe
|
|
XM_017026665.1:c.4263G>C
|
XP_016882154.1:p.Leu1421Phe
|
|
NM_001083961.2:c.4263G>C
MANE Select
|
NP_001077430.1:p.Leu1421Phe
|
|
NM_173636.5:c.4248G>C
|
NP_775907.4:p.Leu1416Phe
|
|