ENST00000236959.14:c.1278G>T
MANE Select
|
ENSP00000236959.9:p.Lys426Asn
|
|
ENST00000236959.13:c.1278G>T
|
ENSP00000236959.9:p.Lys426Asn
|
|
ENST00000426233.1:c.283G>T
|
|
|
ENST00000435675.5:c.1275G>T
|
ENSP00000415935.1:p.Lys425Asn
|
|
ENST00000443953.5:c.*1375G>T
|
ENSP00000406792.1:n.*1375G>T
|
|
ENST00000446622.5:n.358G>T
|
|
|
ENST00000459796.1:n.89G>T
|
|
|
ENST00000467388.1:n.190G>T
|
|
|
ENST00000479093.5:n.193G>T
|
|
|
NM_004044.6:c.1278G>T
|
NP_004035.2:p.Lys426Asn
|
|
XM_017004187.2:c.1278G>T
|
XP_016859676.1:p.Lys426Asn
|
|
XM_024452919.1:c.1101G>T
|
XP_024308687.1:p.Lys367Asn
|
|
NM_004044.7:c.1278G>T
MANE Select
|
NP_004035.2:p.Lys426Asn
|
|