ENST00000688602.1:c.1036T>G
|
|
|
ENST00000689936.1:c.1018T>G
|
|
|
ENST00000359596.8:c.12626T>G
MANE Select
|
ENSP00000352608.2:p.Val4209Gly
|
|
ENST00000355481.8:c.12611T>G
|
ENSP00000347667.3:p.Val4204Gly
|
|
ENST00000359596.7:c.12626T>G
|
ENSP00000352608.2:p.Val4209Gly
|
|
ENST00000360985.7:c.12608T>G
|
ENSP00000354254.4:p.Val4203Gly
|
|
ENST00000594335.5:c.5995T>G
|
|
|
NM_000540.2:c.12626T>G , LRG_766t1:c.12626T>G
|
NP_000531.2:p.Val4209Gly
|
|
NM_001042723.1:c.12611T>G
|
NP_001036188.1:p.Val4204Gly
|
|
XM_006723317.1:c.12608T>G
|
XP_006723380.1:p.Val4203Gly
|
|
XM_006723319.1:c.12593T>G
|
XP_006723382.1:p.Val4198Gly
|
|
XM_011527204.1:c.12623T>G
|
XP_011525506.1:p.Val4208Gly
|
|
XM_011527205.1:c.12626T>G
|
XP_011525507.1:p.Val4209Gly
|
|
XM_006723317.2:c.12608T>G
|
XP_006723380.1:p.Val4203Gly
|
|
XM_006723319.2:c.12593T>G
|
XP_006723382.1:p.Val4198Gly
|
|
XM_011527205.2:c.12626T>G
|
XP_011525507.1:p.Val4209Gly
|
|
NM_000540.3:c.12626T>G
MANE Select
|
NP_000531.2:p.Val4209Gly
|
|
NM_001042723.2:c.12611T>G
|
NP_001036188.1:p.Val4204Gly
|
|