|
ENST00000593677.2:c.1266A>C
|
|
|
|
ENST00000688602.1:c.2663A>C
|
|
|
|
ENST00000689936.1:c.2635A>C
|
|
|
|
ENST00000359596.8:c.14330A>C
MANE Select
|
ENSP00000352608.2:p.Gln4777Pro
|
|
|
ENST00000355481.8:c.14315A>C
|
ENSP00000347667.3:p.Gln4772Pro
|
|
|
ENST00000359596.7:c.14330A>C
|
ENSP00000352608.2:p.Gln4777Pro
|
|
|
ENST00000360985.7:c.14312A>C
|
ENSP00000354254.4:p.Gln4771Pro
|
|
|
NM_000540.2:c.14330A>C , LRG_766t1:c.14330A>C
|
NP_000531.2:p.Gln4777Pro
|
|
|
NM_001042723.1:c.14315A>C
|
NP_001036188.1:p.Gln4772Pro
|
|
|
XM_006723317.1:c.14312A>C
|
XP_006723380.1:p.Gln4771Pro
|
|
|
XM_006723319.1:c.14297A>C
|
XP_006723382.1:p.Gln4766Pro
|
|
|
XM_011527204.1:c.14327A>C
|
XP_011525506.1:p.Gln4776Pro
|
|
|
XM_011527205.1:c.14243A>C
|
XP_011525507.1:p.Gln4748Pro
|
|
|
XM_006723317.2:c.14312A>C
|
XP_006723380.1:p.Gln4771Pro
|
|
|
XM_006723319.2:c.14297A>C
|
XP_006723382.1:p.Gln4766Pro
|
|
|
XM_011527205.2:c.14243A>C
|
XP_011525507.1:p.Gln4748Pro
|
|
|
NM_000540.3:c.14330A>C
MANE Select
|
NP_000531.2:p.Gln4777Pro
|
|
|
NM_001042723.2:c.14315A>C
|
NP_001036188.1:p.Gln4772Pro
|
|
