ENST00000294304.12:c.4607T>A
MANE Select
|
ENSP00000294304.6:p.Met1536Lys
|
|
ENST00000294304.11:c.4607T>A
|
ENSP00000294304.6:p.Met1536Lys
|
|
ENST00000529481.1:n.198T>A
|
|
|
ENST00000529702.1:c.277T>A
|
|
|
ENST00000529993.5:c.*3213T>A
|
ENSP00000436652.1:n.*3213T>A
|
|
NM_001291902.1:c.2864T>A
|
NP_001278831.1:p.Met955Lys
|
|
NM_002335.3:c.4607T>A
|
NP_002326.2:p.Met1536Lys
|
|
XM_005273994.2:c.4721T>A
|
XP_005274051.1:p.Met1574Lys
|
|
XM_011545029.1:c.4748T>A
|
XP_011543331.1:p.Met1583Lys
|
|
XM_011545030.1:c.4634T>A
|
XP_011543332.1:p.Met1545Lys
|
|
XM_011545031.1:c.4764T>A
|
XP_011543333.1:p.Asn1588Lys
|
|
XR_949925.1:n.4994T>A
|
|
|
XR_949926.1:n.5010T>A
|
|
|
XM_017017735.1:c.2978T>A
|
XP_016873224.1:p.Met993Lys
|
|
XM_017017736.1:c.2261T>A
|
XP_016873225.1:p.Met754Lys
|
|
XR_949925.2:n.4994T>A
|
|
|
XR_949926.2:n.5010T>A
|
|
|
NM_002335.4:c.4607T>A
MANE Select
|
NP_002326.2:p.Met1536Lys
|
|
NM_001291902.2:c.2864T>A
|
NP_001278831.1:p.Met955Lys
|
|