ENST00000326003.7:c.758T>G
MANE Select
|
ENSP00000314151.1:p.Ile253Ser
|
|
ENST00000326003.6:c.758T>G
|
ENSP00000314151.1:p.Ile253Ser
|
|
ENST00000360617.7:c.1200T>G
|
ENSP00000353829.2:n.1200T>G
|
|
ENST00000422986.6:c.*414T>G
|
ENSP00000393628.2:n.*414T>G
|
|
ENST00000595392.5:c.*259T>G
|
ENSP00000468912.1:n.*259T>G
|
|
ENST00000595952.5:c.629T>G
|
ENSP00000471155.1:p.Ile210Ser
|
|
ENST00000596333.1:n.936T>G
|
|
|
ENST00000598145.1:c.760T>G
|
|
|
ENST00000601349.5:n.2037T>G
|
|
|
ENST00000601812.1:n.1190T>G
|
|
|
ENST00000617027.4:c.635T>G
|
ENSP00000483513.1:p.Ile212Ser
|
|
NM_001030047.1:c.*483T>G
|
NP_001025218.1:n.*483T>G
|
|
NM_001030048.1:c.629T>G
|
NP_001025219.1:p.Ile210Ser
|
|
NM_001648.2:c.758T>G
MANE Select
|
NP_001639.1:p.Ile253Ser
|
|
XM_011526923.1:c.776T>G
|
XP_011525225.1:p.Ile259Ser
|
|
XR_935817.1:n.1324+845T>G
|
|
|