ENST00000379370.7:c.5035T>C
MANE Select
|
ENSP00000368678.2:p.Tyr1679His
|
|
ENST00000651234.1:c.4720T>C
|
ENSP00000499046.1:p.Tyr1574His
|
|
ENST00000652369.1:c.4720T>C
|
ENSP00000498543.1:p.Tyr1574His
|
|
ENST00000379370.6:c.5035T>C
|
ENSP00000368678.2:p.Tyr1679His
|
|
ENST00000620552.4:c.4621T>C
|
ENSP00000484607.1:p.Tyr1541His
|
|
NM_001305275.1:c.5035T>C
|
NP_001292204.1:p.Tyr1679His
|
|
NM_198576.3:c.5035T>C
|
NP_940978.2:p.Tyr1679His
|
|
XM_005244749.2:c.5035T>C
|
XP_005244806.1:p.Tyr1679His
|
|
XM_006710635.2:c.5035T>C
|
XP_006710698.1:p.Tyr1679His
|
|
XM_011541429.1:c.5035T>C
|
XP_011539731.1:p.Tyr1679His
|
|
XM_011541430.1:c.4162T>C
|
XP_011539732.1:p.Tyr1388His
|
|
XM_011541431.1:c.3301T>C
|
XP_011539733.1:p.Tyr1101His
|
|
XR_946650.1:n.5102T>C
|
|
|
NM_001364727.1:c.4720T>C
|
NP_001351656.1:p.Tyr1574His
|
|
XM_005244749.3:c.5035T>C
|
XP_005244806.1:p.Tyr1679His
|
|
XM_011541429.2:c.5035T>C
|
XP_011539731.1:p.Tyr1679His
|
|
XR_946650.2:n.5106T>C
|
|
|
NM_001305275.2:c.5035T>C
|
NP_001292204.1:p.Tyr1679His
|
|
NM_198576.4:c.5035T>C
MANE Select
|
NP_940978.2:p.Tyr1679His
|
|
NM_001364727.2:c.4720T>C
|
NP_001351656.1:p.Tyr1574His
|
|