ENST00000681617.1:c.428T>A
|
ENSP00000505544.1:p.Leu143Ter
|
|
ENST00000681780.1:c.-116T>A
|
ENSP00000505780.1:n.-116T>A
|
|
ENST00000370131.3:c.428T>A
|
ENSP00000359150.3:p.Leu143Ter
|
|
ENST00000370132.8:c.428T>A
MANE Select
|
ENSP00000359151.3:p.Leu143Ter
|
|
NM_001918.3:c.428T>A
|
NP_001909.3:p.Leu143Ter
|
|
XM_005270545.2:c.-116T>A
|
XP_005270602.1:n.-116T>A
|
|
XM_005270546.2:c.-111+4698T>A
|
XP_005270603.1:n.-111+4698T>A
|
|
XR_946560.1:n.448T>A
|
|
|
XM_005270545.4:c.-116T>A
|
XP_005270602.1:n.-116T>A
|
|
XM_017000468.2:c.-116T>A
|
XP_016855957.1:n.-116T>A
|
|
XM_017000469.2:c.-111+4698T>A
|
XP_016855958.1:n.-111+4698T>A
|
|
XR_946560.3:n.445T>A
|
|
|
NM_001918.4:c.428T>A
|
NP_001909.3:p.Leu143Ter
|
|
NM_001918.5:c.428T>A
MANE Select
|
NP_001909.4:p.Leu143Ter
|
|
NM_001399969.1:c.-116T>A
|
NP_001386898.1:n.-116T>A
|
|
NM_001399972.1:c.-116T>A
|
NP_001386901.1:n.-116T>A
|
|
NR_174363.1:n.265+4698T>A
|
|
|
NR_174364.1:n.442T>A
|
|
|
NR_174365.1:n.442T>A
|
|
|
NR_174366.1:n.442T>A
|
|
|