ENST00000326003.7:c.762G>T
MANE Select
|
ENSP00000314151.1:p.Lys254Asn
|
|
ENST00000326003.6:c.762G>T
|
ENSP00000314151.1:p.Lys254Asn
|
|
ENST00000360617.7:c.1204G>T
|
ENSP00000353829.2:n.1204G>T
|
|
ENST00000422986.6:c.*418G>T
|
ENSP00000393628.2:n.*418G>T
|
|
ENST00000595392.5:c.*263G>T
|
ENSP00000468912.1:n.*263G>T
|
|
ENST00000595952.5:c.633G>T
|
ENSP00000471155.1:p.Lys211Asn
|
|
ENST00000596333.1:n.940G>T
|
|
|
ENST00000598145.1:c.764G>T
|
|
|
ENST00000601349.5:n.2041G>T
|
|
|
ENST00000601812.1:n.1194G>T
|
|
|
ENST00000617027.4:c.639G>T
|
ENSP00000483513.1:p.Lys213Asn
|
|
NM_001030047.1:c.*487G>T
|
NP_001025218.1:n.*487G>T
|
|
NM_001030048.1:c.633G>T
|
NP_001025219.1:p.Lys211Asn
|
|
NM_001648.2:c.762G>T
MANE Select
|
NP_001639.1:p.Lys254Asn
|
|
XM_011526923.1:c.780G>T
|
XP_011525225.1:p.Lys260Asn
|
|
XR_935817.1:n.1324+849G>T
|
|
|