ENST00000403559.9:c.1753G>T
|
ENSP00000385069.4:p.Val585Phe
|
|
ENST00000703612.1:c.1693G>T
|
ENSP00000515396.1:p.Val565Phe
|
|
ENST00000703613.1:c.1753G>T
|
ENSP00000515397.1:p.Val585Phe
|
|
ENST00000703614.1:c.1702G>T
|
ENSP00000515398.1:p.Val568Phe
|
|
ENST00000703616.1:c.1828G>T
|
ENSP00000515400.1:p.Val610Phe
|
|
ENST00000703617.1:c.1147G>T
|
ENSP00000515401.1:p.Val383Phe
|
|
ENST00000703618.1:c.599G>T
|
|
|
ENST00000350908.9:c.1702G>T
MANE Select
|
ENSP00000265436.7:p.Val568Phe
|
|
ENST00000393489.8:c.*1496G>T
|
ENSP00000377129.4:n.*1496G>T
|
|
ENST00000350908.8:c.1702G>T
|
ENSP00000265436.7:p.Val568Phe
|
|
ENST00000393489.7:c.1426G>T
|
ENSP00000377129.3:p.Val476Phe
|
|
ENST00000393491.7:c.1147G>T
|
ENSP00000377130.3:p.Val383Phe
|
|
ENST00000393494.6:c.1702G>T
|
ENSP00000377132.2:p.Val568Phe
|
|
ENST00000393498.6:c.1639G>T
|
ENSP00000377135.2:p.Val547Phe
|
|
ENST00000403559.8:c.1753G>T
|
ENSP00000385069.4:p.Val585Phe
|
|
ENST00000408937.7:c.1777G>T
|
ENSP00000386200.3:p.Val593Phe
|
|
ENST00000412402.5:c.*1420G>T
|
ENSP00000405470.1:n.*1420G>T
|
|
ENST00000441290.6:c.*1702G>T
|
ENSP00000416825.1:n.*1702G>T
|
|
ENST00000634411.1:c.1651G>T
|
ENSP00000489135.1:p.Val551Phe
|
|
ENST00000634623.1:c.1642G>T
|
ENSP00000488944.1:p.Val548Phe
|
|
ENST00000634664.1:n.177G>T
|
|
|
ENST00000635109.1:c.*1499G>T
|
ENSP00000489457.1:n.*1499G>T
|
|
ENST00000635534.1:c.1693G>T
|
ENSP00000489229.1:p.Val565Phe
|
|
ENST00000635638.1:c.1705G>T
|
ENSP00000489073.1:p.Val569Phe
|
|
NM_001172766.2:c.1699G>T
|
NP_001166237.1:p.Val567Phe
|
|
NM_014491.3:c.1702G>T
|
NP_055306.1:p.Val568Phe
|
|
NM_148898.3:c.1777G>T
|
NP_683696.2:p.Val593Phe
|
|
NM_148900.3:c.1753G>T
|
NP_683698.2:p.Val585Phe
|
|
NR_033766.1:n.2087G>T
|
|
|
NR_033767.1:n.2134G>T
|
|
|
XM_011516706.1:c.1846G>T
|
XP_011515008.1:p.Val616Phe
|
|
XM_017012801.2:c.1777G>T
|
XP_016868290.1:p.Val593Phe
|
|
NM_014491.4:c.1702G>T
MANE Select
|
NP_055306.1:p.Val568Phe
|
|
NM_001172766.3:c.1699G>T
|
NP_001166237.1:p.Val567Phe
|
|
NM_148898.4:c.1777G>T
|
NP_683696.2:p.Val593Phe
|
|
NR_033766.2:n.2070G>T
|
|
|
NR_033767.2:n.2316G>T
|
|
|
NM_148900.4:c.1753G>T
|
NP_683698.2:p.Val585Phe
|
|