ENST00000471476.2:c.*1345T>A
|
ENSP00000497663.1:n.*1345T>A
|
|
ENST00000647645.1:c.1703T>A
|
ENSP00000497450.1:p.Ile568Lys
|
|
ENST00000647730.1:c.*1456T>A
|
ENSP00000497781.1:n.*1456T>A
|
|
ENST00000647788.1:c.*910T>A
|
ENSP00000497769.1:n.*910T>A
|
|
ENST00000648271.1:c.*2232T>A
|
ENSP00000497795.1:n.*2232T>A
|
|
ENST00000648807.1:c.1613T>A
|
ENSP00000497472.1:p.Ile538Lys
|
|
ENST00000648960.1:c.1283T>A
|
ENSP00000497091.1:p.Ile428Lys
|
|
ENST00000649067.1:c.*769T>A
|
ENSP00000497052.1:n.*769T>A
|
|
ENST00000649689.2:c.1766T>A
MANE Select
|
ENSP00000497569.1:p.Ile589Lys
|
|
ENST00000361951.4:c.1766T>A
|
ENSP00000355086.4:p.Ile589Lys
|
|
ENST00000471476.1:n.588T>A
|
|
|
NM_018122.4:c.1766T>A
|
NP_060592.2:p.Ile589Lys
|
|
XM_006711427.2:c.1613T>A
|
XP_006711490.1:p.Ile538Lys
|
|
NM_001365212.1:c.1613T>A
|
NP_001352141.1:p.Ile538Lys
|
|
NM_018122.5:c.1766T>A
MANE Select
|
NP_060592.2:p.Ile589Lys
|
|