ENST00000317961.9:c.3521T>G
MANE Select
|
ENSP00000322408.4:p.Ile1174Ser
|
|
ENST00000317961.8:c.3521T>G
|
ENSP00000322408.4:p.Ile1174Ser
|
|
ENST00000382806.6:c.3350T>G
|
ENSP00000372256.2:p.Ile1117Ser
|
|
ENST00000415360.1:c.437T>G
|
ENSP00000389433.1:p.Ile146Ser
|
|
ENST00000440077.5:c.3398T>G
|
ENSP00000398543.1:p.Ile1133Ser
|
|
ENST00000469599.6:n.2119T>G
|
|
|
ENST00000492117.1:n.3413T>G
|
|
|
ENST00000541639.5:c.3614T>G
|
ENSP00000444293.1:p.Ile1205Ser
|
|
NM_001146705.1:c.3614T>G
|
NP_001140177.1:p.Ile1205Ser
|
|
NM_001146706.1:c.3350T>G
|
NP_001140178.1:p.Ile1117Ser
|
|
NM_004653.4:c.3521T>G
|
NP_004644.2:p.Ile1174Ser
|
|
XM_005262560.1:c.3386T>G
|
XP_005262617.1:p.Ile1129Ser
|
|
XM_005262561.1:c.3290T>G
|
XP_005262618.1:p.Ile1097Ser
|
|
XM_011531468.1:c.3443T>G
|
XP_011529770.1:p.Ile1148Ser
|
|
XR_244571.2:n.3809T>G
|
|
|
XR_430568.2:n.4143T>G
|
|
|
XM_005262560.3:c.3386T>G
|
XP_005262617.1:p.Ile1129Ser
|
|
XM_005262561.3:c.3290T>G
|
XP_005262618.1:p.Ile1097Ser
|
|
XM_011531468.3:c.3443T>G
|
XP_011529770.1:p.Ile1148Ser
|
|
XM_024452495.1:c.1511T>G
|
XP_024308263.1:p.Ile504Ser
|
|
XM_024452496.1:c.1277T>G
|
XP_024308264.1:p.Ile426Ser
|
|
XR_001756009.2:n.4259T>G
|
|
|
XR_001756010.2:n.4259T>G
|
|
|
XR_001756011.2:n.4124T>G
|
|
|
XR_001756012.2:n.4272T>G
|
|
|
XR_001756013.2:n.3590T>G
|
|
|
XR_002958832.1:n.3691T>G
|
|
|
XR_002958834.1:n.3915T>G
|
|
|
XR_002958835.1:n.3798T>G
|
|
|
XR_002958836.1:n.4481T>G
|
|
|
XR_002958837.1:n.4288T>G
|
|
|
XR_244571.4:n.3808T>G
|
|
|
XR_430568.4:n.4142T>G
|
|
|
NM_001146706.2:c.3350T>G
|
NP_001140178.1:p.Ile1117Ser
|
|
NM_004653.5:c.3521T>G
MANE Select
|
NP_004644.2:p.Ile1174Ser
|
|
NM_001146705.2:c.3614T>G
|
NP_001140177.1:p.Ile1205Ser
|
|