ENST00000326003.7:c.770T>C
MANE Select
|
ENSP00000314151.1:p.Ile257Thr
|
|
ENST00000326003.6:c.770T>C
|
ENSP00000314151.1:p.Ile257Thr
|
|
ENST00000360617.7:c.1212T>C
|
ENSP00000353829.2:n.1212T>C
|
|
ENST00000422986.6:c.*426T>C
|
ENSP00000393628.2:n.*426T>C
|
|
ENST00000595392.5:c.*271T>C
|
ENSP00000468912.1:n.*271T>C
|
|
ENST00000595952.5:c.641T>C
|
ENSP00000471155.1:p.Ile214Thr
|
|
ENST00000596333.1:n.948T>C
|
|
|
ENST00000598145.1:c.772T>C
|
|
|
ENST00000601349.5:n.2049T>C
|
|
|
ENST00000601812.1:n.1202T>C
|
|
|
ENST00000617027.4:c.647T>C
|
ENSP00000483513.1:p.Ile216Thr
|
|
NM_001030047.1:c.*495T>C
|
NP_001025218.1:n.*495T>C
|
|
NM_001030048.1:c.641T>C
|
NP_001025219.1:p.Ile214Thr
|
|
NM_001648.2:c.770T>C
MANE Select
|
NP_001639.1:p.Ile257Thr
|
|
XM_011526923.1:c.788T>C
|
XP_011525225.1:p.Ile263Thr
|
|
XR_935817.1:n.1324+857T>C
|
|
|