ENST00000593677.2:c.1957+780G>A
|
|
|
ENST00000688602.1:c.3386G>A
|
|
|
ENST00000689936.1:c.3358G>A
|
|
|
ENST00000692547.1:n.446G>A
|
|
|
ENST00000359596.8:c.15053G>A
MANE Select
|
ENSP00000352608.2:p.Arg5018Lys
|
|
ENST00000355481.8:c.15038G>A
|
ENSP00000347667.3:p.Arg5013Lys
|
|
ENST00000359596.7:c.15053G>A
|
ENSP00000352608.2:p.Arg5018Lys
|
|
ENST00000360985.7:c.15035G>A
|
ENSP00000354254.4:p.Arg5012Lys
|
|
NM_000540.2:c.15053G>A , LRG_766t1:c.15053G>A
|
NP_000531.2:p.Arg5018Lys
|
|
NM_001042723.1:c.15038G>A
|
NP_001036188.1:p.Arg5013Lys
|
|
XM_006723317.1:c.15035G>A
|
XP_006723380.1:p.Arg5012Lys
|
|
XM_006723319.1:c.15020G>A
|
XP_006723382.1:p.Arg5007Lys
|
|
XM_011527204.1:c.15050G>A
|
XP_011525506.1:p.Arg5017Lys
|
|
XM_011527205.1:c.14966G>A
|
XP_011525507.1:p.Arg4989Lys
|
|
XM_006723317.2:c.15035G>A
|
XP_006723380.1:p.Arg5012Lys
|
|
XM_006723319.2:c.15020G>A
|
XP_006723382.1:p.Arg5007Lys
|
|
XM_011527205.2:c.14966G>A
|
XP_011525507.1:p.Arg4989Lys
|
|
NM_000540.3:c.15053G>A
MANE Select
|
NP_000531.2:p.Arg5018Lys
|
|
NM_001042723.2:c.15038G>A
|
NP_001036188.1:p.Arg5013Lys
|
|