ENST00000281928.9:c.1249C>A
MANE Select
|
ENSP00000281928.3:p.Pro417Thr
|
|
ENST00000548743.2:c.1219C>A
|
ENSP00000448553.2:p.Pro407Thr
|
|
ENST00000549786.2:c.677C>A
|
|
|
ENST00000647567.1:c.1156C>A
|
ENSP00000497136.1:p.Pro386Thr
|
|
ENST00000648737.1:n.1013C>A
|
|
|
ENST00000650226.1:c.1249C>A
|
ENSP00000496981.1:p.Pro417Thr
|
|
ENST00000281928.7:c.1249C>A
|
ENSP00000281928.3:p.Pro417Thr
|
|
NM_015335.4:c.1249C>A
|
NP_056150.1:p.Pro417Thr
|
|
XM_011538080.1:c.1249C>A
|
XP_011536382.1:p.Pro417Thr
|
|
XM_011538081.1:c.1249C>A
|
XP_011536383.1:p.Pro417Thr
|
|
XM_011538082.1:c.1219C>A
|
XP_011536384.1:p.Pro407Thr
|
|
XM_011538080.2:c.1249C>A
|
XP_011536382.1:p.Pro417Thr
|
|
XM_011538081.2:c.1249C>A
|
XP_011536383.1:p.Pro417Thr
|
|
XM_011538082.2:c.1219C>A
|
XP_011536384.1:p.Pro407Thr
|
|
XM_017019090.1:c.1249C>A
|
XP_016874579.1:p.Pro417Thr
|
|
NM_015335.5:c.1249C>A
MANE Select
|
NP_056150.1:p.Pro417Thr
|
|