ENST00000527168.6:n.333-1G>T
|
|
|
ENST00000529110.2:c.318-1G>T
|
ENSP00000435349.2:n.318-1G>T
|
|
ENST00000529957.6:n.292-1G>T
|
|
|
ENST00000683366.1:c.179-1G>T
|
ENSP00000507283.1:n.179-1G>T
|
|
ENST00000683887.1:c.282-1G>T
|
ENSP00000506886.1:n.282-1G>T
|
|
ENST00000684100.1:n.227G>T
|
|
|
ENST00000684126.1:n.292-1G>T
|
|
|
ENST00000684688.1:n.859-1G>T
|
|
|
ENST00000204679.9:c.234-1G>T
MANE Select
|
ENSP00000204679.4:n.234-1G>T
|
|
ENST00000204679.8:c.234-1G>T
|
ENSP00000204679.4:n.234-1G>T
|
|
ENST00000526820.5:c.*136-1G>T
|
ENSP00000434413.1:n.*136-1G>T
|
|
ENST00000527076.1:n.1249G>T
|
|
|
ENST00000527168.5:n.270-1G>T
|
|
|
ENST00000529110.1:c.301-1G>T
|
|
|
ENST00000529957.5:n.333-1G>T
|
|
|
NM_032520.4:c.234-1G>T
|
NP_115909.1:n.234-1G>T
|
|
XM_017023782.1:c.282-1G>T
|
XP_016879271.1:n.282-1G>T
|
|
XM_017023783.1:c.-127-1G>T
|
XP_016879272.1:n.-127-1G>T
|
|
NM_032520.5:c.234-1G>T
MANE Select
|
NP_115909.1:n.234-1G>T
|
|