ENST00000262352.8:c.1111G>T
(SLC1A1)
MANE Select
|
ENSP00000262352.3:p.Ala371Ser
|
|
ENST00000262352.7:c.1111G>T
(SLC1A1)
|
ENSP00000262352.3:p.Ala371Ser
|
|
ENST00000422398.1:c.398G>T
(SLC1A1)
|
|
|
ENST00000485616.5:c.*782-22293C>A
(SPATA6L)
|
ENSP00000420003.1:n.*782-22293C>A
|
|
NM_004170.5:c.1111G>T
(SLC1A1)
|
NP_004161.4:p.Ala371Ser
|
|
XM_011518007.1:c.1180G>T
(SLC1A1)
|
XP_011516309.1:p.Ala394Ser
|
|
XM_011518008.1:c.1120G>T
(SLC1A1)
|
XP_011516310.1:p.Ala374Ser
|
|
XM_011518009.1:c.1051G>T
(SLC1A1)
|
XP_011516311.1:p.Ala351Ser
|
|
XM_011518010.1:c.970G>T
(SLC1A1)
|
XP_011516312.1:p.Ala324Ser
|
|
XM_011518008.3:c.1120G>T
(SLC1A1)
|
XP_011516310.1:p.Ala374Ser
|
|
XM_011518009.3:c.1051G>T
(SLC1A1)
|
XP_011516311.1:p.Ala351Ser
|
|
XM_017014882.2:c.*1+27498C>A
(SPATA6L)
|
XP_016870371.1:n.*1+27498C>A
|
|
XM_017015042.1:c.1072G>T
(SLC1A1)
|
XP_016870531.1:p.Ala358Ser
|
|
XM_017015043.1:c.1003G>T
(SLC1A1)
|
XP_016870532.1:p.Ala335Ser
|
|
XR_001746335.2:n.1478+23972C>A
(SPATA6L)
|
|
|
NM_004170.6:c.1111G>T
(SLC1A1)
MANE Select
|
NP_004161.4:p.Ala371Ser
|
|