ENST00000294304.12:c.4499C>A
MANE Select
|
ENSP00000294304.6:p.Pro1500Gln
|
|
ENST00000294304.11:c.4499C>A
|
ENSP00000294304.6:p.Pro1500Gln
|
|
ENST00000529702.1:c.169C>A
|
|
|
ENST00000529993.5:c.*3105C>A
|
ENSP00000436652.1:n.*3105C>A
|
|
NM_001291902.1:c.2756C>A
|
NP_001278831.1:p.Pro919Gln
|
|
NM_002335.3:c.4499C>A
|
NP_002326.2:p.Pro1500Gln
|
|
XM_005273994.2:c.4613C>A
|
XP_005274051.1:p.Pro1538Gln
|
|
XM_011545029.1:c.4640C>A
|
XP_011543331.1:p.Pro1547Gln
|
|
XM_011545030.1:c.4526C>A
|
XP_011543332.1:p.Pro1509Gln
|
|
XM_011545031.1:c.4656C>A
|
XP_011543333.1:p.Pro1552=
|
|
XR_949925.1:n.4655C>A
|
|
|
XR_949926.1:n.4671C>A
|
|
|
XM_017017735.1:c.2870C>A
|
XP_016873224.1:p.Pro957Gln
|
|
XM_017017736.1:c.2153C>A
|
XP_016873225.1:p.Pro718Gln
|
|
XR_949925.2:n.4655C>A
|
|
|
XR_949926.2:n.4671C>A
|
|
|
NM_002335.4:c.4499C>A
MANE Select
|
NP_002326.2:p.Pro1500Gln
|
|
NM_001291902.2:c.2756C>A
|
NP_001278831.1:p.Pro919Gln
|
|