ENST00000593677.2:c.1497T>A
|
|
|
ENST00000688602.1:c.2894T>A
|
|
|
ENST00000689936.1:c.2866T>A
|
|
|
ENST00000359596.8:c.14561T>A
MANE Select
|
ENSP00000352608.2:p.Val4854Glu
|
|
ENST00000355481.8:c.14546T>A
|
ENSP00000347667.3:p.Val4849Glu
|
|
ENST00000359596.7:c.14561T>A
|
ENSP00000352608.2:p.Val4854Glu
|
|
ENST00000360985.7:c.14543T>A
|
ENSP00000354254.4:p.Val4848Glu
|
|
NM_000540.2:c.14561T>A , LRG_766t1:c.14561T>A
|
NP_000531.2:p.Val4854Glu
|
|
NM_001042723.1:c.14546T>A
|
NP_001036188.1:p.Val4849Glu
|
|
XM_006723317.1:c.14543T>A
|
XP_006723380.1:p.Val4848Glu
|
|
XM_006723319.1:c.14528T>A
|
XP_006723382.1:p.Val4843Glu
|
|
XM_011527204.1:c.14558T>A
|
XP_011525506.1:p.Val4853Glu
|
|
XM_011527205.1:c.14474T>A
|
XP_011525507.1:p.Val4825Glu
|
|
XM_006723317.2:c.14543T>A
|
XP_006723380.1:p.Val4848Glu
|
|
XM_006723319.2:c.14528T>A
|
XP_006723382.1:p.Val4843Glu
|
|
XM_011527205.2:c.14474T>A
|
XP_011525507.1:p.Val4825Glu
|
|
NM_000540.3:c.14561T>A
MANE Select
|
NP_000531.2:p.Val4854Glu
|
|
NM_001042723.2:c.14546T>A
|
NP_001036188.1:p.Val4849Glu
|
|