ENST00000593677.2:c.862C>A
|
|
|
ENST00000688602.1:c.2259C>A
|
|
|
ENST00000689936.1:c.2231C>A
|
|
|
ENST00000359596.8:c.13926C>A
MANE Select
|
ENSP00000352608.2:p.Pro4642=
|
|
ENST00000355481.8:c.13911C>A
|
ENSP00000347667.3:p.Pro4637=
|
|
ENST00000359596.7:c.13926C>A
|
ENSP00000352608.2:p.Pro4642=
|
|
ENST00000360985.7:c.13908C>A
|
ENSP00000354254.4:p.Pro4636=
|
|
ENST00000593677.1:c.386C>A
|
|
|
NM_000540.2:c.13926C>A , LRG_766t1:c.13926C>A
|
NP_000531.2:p.Pro4642=
|
|
NM_001042723.1:c.13911C>A
|
NP_001036188.1:p.Pro4637=
|
|
XM_006723317.1:c.13908C>A
|
XP_006723380.1:p.Pro4636=
|
|
XM_006723319.1:c.13893C>A
|
XP_006723382.1:p.Pro4631=
|
|
XM_011527204.1:c.13923C>A
|
XP_011525506.1:p.Pro4641=
|
|
XM_011527205.1:c.13839C>A
|
XP_011525507.1:p.Pro4613=
|
|
XM_006723317.2:c.13908C>A
|
XP_006723380.1:p.Pro4636=
|
|
XM_006723319.2:c.13893C>A
|
XP_006723382.1:p.Pro4631=
|
|
XM_011527205.2:c.13839C>A
|
XP_011525507.1:p.Pro4613=
|
|
NM_000540.3:c.13926C>A
MANE Select
|
NP_000531.2:p.Pro4642=
|
|
NM_001042723.2:c.13911C>A
|
NP_001036188.1:p.Pro4637=
|
|