|
ENST00000420291.3:c.1363C>T
|
ENSP00000416728.3:p.Arg455Ter
|
|
|
ENST00000424362.7:c.1363C>T
|
ENSP00000398863.2:p.Arg455Ter
|
|
|
ENST00000426583.2:c.1363C>T
|
ENSP00000404235.2:p.Arg455Ter
|
|
|
ENST00000457855.2:c.1363C>T
|
ENSP00000410210.2:p.Arg455Ter
|
|
|
ENST00000672126.2:c.1363C>T
|
ENSP00000500718.1:p.Arg455Ter
|
|
|
ENST00000672515.2:c.1363C>T
|
ENSP00000499951.2:p.Arg455Ter
|
|
|
ENST00000673551.2:c.1363C>T
|
ENSP00000500672.1:p.Arg455Ter
|
|
|
ENST00000682208.1:c.1363C>T
|
ENSP00000508123.1:p.Arg455Ter
|
|
|
ENST00000682980.1:c.1363C>T
|
ENSP00000508198.1:p.Arg455Ter
|
|
|
ENST00000683423.1:c.1363C>T
|
ENSP00000507659.1:p.Arg455Ter
|
|
|
ENST00000683639.1:c.1363C>T
|
ENSP00000506903.1:p.Arg455Ter
|
|
|
ENST00000683743.1:c.1363C>T
|
ENSP00000507469.1:p.Arg455Ter
|
|
|
ENST00000684199.1:c.1363C>T
|
ENSP00000506921.1:p.Arg455Ter
|
|
|
ENST00000684206.1:c.1363C>T
|
ENSP00000507148.1:p.Arg455Ter
|
|
|
ENST00000684223.1:c.1363C>T
|
ENSP00000506789.1:p.Arg455Ter
|
|
|
ENST00000684333.1:c.1363C>T
|
ENSP00000508256.1:p.Arg455Ter
|
|
|
ENST00000684608.1:c.1363C>T
|
ENSP00000507969.1:p.Arg455Ter
|
|
|
ENST00000383829.7:c.1363C>T
MANE Select
|
ENSP00000373340.2:p.Arg455Ter
|
|
|
ENST00000424362.6:c.1363C>T
|
ENSP00000398863.1:p.Arg455Ter
|
|
|
ENST00000672126.1:c.1363C>T
|
ENSP00000500718.1:p.Arg455Ter
|
|
|
ENST00000672515.1:c.1355C>T
|
|
|
|
ENST00000673551.1:c.1363C>T
|
ENSP00000500672.1:p.Arg455Ter
|
|
|
ENST00000383829.6:c.1363C>T
|
ENSP00000373340.2:p.Arg455Ter
|
|
|
ENST00000424362.5:c.1363C>T
|
ENSP00000398863.1:p.Arg455Ter
|
|
|
ENST00000433861.6:c.1363C>T
|
ENSP00000402485.2:p.Arg455Ter
|
|
|
ENST00000457855.1:c.1363C>T
|
ENSP00000410210.1:p.Arg455Ter
|
|
|
NM_001003694.1:c.1363C>T
|
NP_001003694.1:p.Arg455Ter
|
|
|
NM_004634.2:c.1363C>T
|
NP_004625.2:p.Arg455Ter
|
|
|
XM_005265449.1:c.1363C>T
|
XP_005265506.1:p.Arg455Ter
|
|
|
XM_005265450.1:c.1363C>T
|
XP_005265507.1:p.Arg455Ter
|
|
|
XM_005265451.1:c.1363C>T
|
XP_005265508.1:p.Arg455Ter
|
|
|
XM_005265452.1:c.1363C>T
|
XP_005265509.1:p.Arg455Ter
|
|
|
XM_005265453.1:c.1363C>T
|
XP_005265510.1:p.Arg455Ter
|
|
|
XM_005265454.1:c.1363C>T
|
XP_005265511.1:p.Arg455Ter
|
|
|
XM_011534101.1:c.1363C>T
|
XP_011532403.1:p.Arg455Ter
|
|
|
XM_011534102.1:c.1363C>T
|
XP_011532404.1:p.Arg455Ter
|
|
|
NM_001319049.1:c.1363C>T
|
NP_001305978.1:p.Arg455Ter
|
|
|
NM_001319050.1:c.1363C>T
|
NP_001305979.1:p.Arg455Ter
|
|
|
XM_024453741.1:c.1363C>T
|
XP_024309509.1:p.Arg455Ter
|
|
|
XM_024453742.1:c.1363C>T
|
XP_024309510.1:p.Arg455Ter
|
|
|
XM_024453743.1:c.1363C>T
|
XP_024309511.1:p.Arg455Ter
|
|
|
XM_024453744.1:c.1363C>T
|
XP_024309512.1:p.Arg455Ter
|
|
|
XR_001740257.1:n.1783C>T
|
|
|
|
XR_001740258.1:n.1783C>T
|
|
|
|
NM_001003694.2:c.1363C>T
MANE Select
|
NP_001003694.1:p.Arg455Ter
|
|
|
NR_160918.1:n.1777C>T
|
|
|
|
NM_001319049.2:c.1363C>T
|
NP_001305978.1:p.Arg455Ter
|
|
|
NM_001319050.2:c.1363C>T
|
NP_001305979.1:p.Arg455Ter
|
|
|
NM_004634.3:c.1363C>T
|
NP_004625.2:p.Arg455Ter
|
|
