ENST00000700559.2:c.1386G>T
|
ENSP00000515065.2:p.Leu462=
|
|
ENST00000700563.2:c.1386G>T
|
ENSP00000515066.2:p.Leu462=
|
|
ENST00000700559.1:c.601G>T
|
|
|
ENST00000700560.1:n.601G>T
|
|
|
ENST00000700561.1:n.727G>T
|
|
|
ENST00000700563.1:c.1340G>T
|
|
|
ENST00000700564.1:n.1390G>T
|
|
|
ENST00000700565.1:n.1239G>T
|
|
|
ENST00000070846.11:c.1518G>T
|
ENSP00000070846.6:p.Leu506=
|
|
ENST00000340811.9:c.1386G>T
MANE Select
|
ENSP00000342800.5:p.Leu462=
|
|
ENST00000070846.10:c.1518G>T
|
ENSP00000070846.6:p.Leu506=
|
|
ENST00000340811.8:c.1386G>T
|
ENSP00000342800.4:p.Leu462=
|
|
ENST00000613243.1:c.1518G>T
|
ENSP00000478295.1:p.Leu506=
|
|
NM_001005242.2:c.1386G>T
|
NP_001005242.2:p.Leu462=
|
|
NM_004572.3:c.1518G>T , LRG_398t1:c.1518G>T
|
NP_004563.2:p.Leu506=
|
|
NM_001005242.3:c.1386G>T
MANE Select
|
NP_001005242.2:p.Leu462=
|
|
NM_004572.4:c.1518G>T
|
NP_004563.2:p.Leu506=
|
|