ENST00000379370.7:c.1822G>T
MANE Select
|
ENSP00000368678.2:p.Ala608Ser
|
|
ENST00000651234.1:c.1507G>T
|
ENSP00000499046.1:p.Ala503Ser
|
|
ENST00000652369.1:c.1507G>T
|
ENSP00000498543.1:p.Ala503Ser
|
|
ENST00000379370.6:c.1822G>T
|
ENSP00000368678.2:p.Ala608Ser
|
|
ENST00000620552.4:c.1408G>T
|
ENSP00000484607.1:p.Ala470Ser
|
|
NM_001305275.1:c.1822G>T
|
NP_001292204.1:p.Ala608Ser
|
|
NM_198576.3:c.1822G>T
|
NP_940978.2:p.Ala608Ser
|
|
XM_005244749.2:c.1822G>T
|
XP_005244806.1:p.Ala608Ser
|
|
XM_006710635.2:c.1822G>T
|
XP_006710698.1:p.Ala608Ser
|
|
XM_011541429.1:c.1822G>T
|
XP_011539731.1:p.Ala608Ser
|
|
XM_011541430.1:c.949G>T
|
XP_011539732.1:p.Ala317Ser
|
|
XM_011541431.1:c.88G>T
|
XP_011539733.1:p.Ala30Ser
|
|
XR_946650.1:n.1889G>T
|
|
|
NM_001364727.1:c.1507G>T
|
NP_001351656.1:p.Ala503Ser
|
|
XM_005244749.3:c.1822G>T
|
XP_005244806.1:p.Ala608Ser
|
|
XM_011541429.2:c.1822G>T
|
XP_011539731.1:p.Ala608Ser
|
|
XR_946650.2:n.1893G>T
|
|
|
NM_001305275.2:c.1822G>T
|
NP_001292204.1:p.Ala608Ser
|
|
NM_198576.4:c.1822G>T
MANE Select
|
NP_940978.2:p.Ala608Ser
|
|
NM_001364727.2:c.1507G>T
|
NP_001351656.1:p.Ala503Ser
|
|