ENST00000366963.9:c.1480T>G
MANE Select
|
ENSP00000355930.4:p.Leu494Val
|
|
ENST00000324965.8:c.1386-1083T>G
|
ENSP00000318103.4:n.1386-1083T>G
|
|
ENST00000366963.8:c.1480T>G
|
ENSP00000355930.4:p.Leu494Val
|
|
ENST00000457470.6:c.1386-3624T>G
|
ENSP00000409557.2:n.1386-3624T>G
|
|
ENST00000460902.2:c.1265T>G
|
ENSP00000439274.1:n.1265T>G
|
|
ENST00000539263.5:c.*953T>G
|
ENSP00000443245.1:n.*953T>G
|
|
NM_003057.2:c.1480T>G
|
NP_003048.1:p.Leu494Val
|
|
NM_153187.1:c.1386-1083T>G
|
NP_694857.1:n.1386-1083T>G
|
|
XM_005267102.3:c.1480T>G
|
XP_005267159.1:p.Leu494Val
|
|
XM_005267103.1:c.1480T>G
|
XP_005267160.1:p.Leu494Val
|
|
XM_005267104.3:c.904T>G
|
XP_005267161.1:p.Leu302Val
|
|
XM_005267105.3:c.904T>G
|
XP_005267162.1:p.Leu302Val
|
|
XM_006715552.1:c.1386-3624T>G
|
XP_006715615.1:n.1386-3624T>G
|
|
XM_011536074.1:c.904T>G
|
XP_011534376.1:p.Leu302Val
|
|
XM_005267102.5:c.1480T>G
|
XP_005267159.1:p.Leu494Val
|
|
XM_005267103.2:c.1480T>G
|
XP_005267160.1:p.Leu494Val
|
|
XM_005267104.5:c.904T>G
|
XP_005267161.1:p.Leu302Val
|
|
XM_005267105.5:c.904T>G
|
XP_005267162.1:p.Leu302Val
|
|
XM_006715552.2:c.1386-3624T>G
|
XP_006715615.1:n.1386-3624T>G
|
|
XM_011536074.3:c.904T>G
|
XP_011534376.1:p.Leu302Val
|
|
NM_003057.3:c.1480T>G
MANE Select
|
NP_003048.1:p.Leu494Val
|
|
NM_153187.2:c.1386-1083T>G
|
NP_694857.1:n.1386-1083T>G
|
|