ENST00000299314.12:c.3242C=
MANE Select
|
ENSP00000299314.7:p.Pro1081=
|
|
ENST00000299314.11:c.3242C=
|
ENSP00000299314.7:p.Pro1081=
|
|
ENST00000549194.1:n.108C=
|
|
|
ENST00000550718.1:c.54C=
|
|
|
NM_024312.4:c.3242C=
|
NP_077288.2:p.Pro1081=
|
|
XM_006719593.2:c.3242C=
|
XP_006719656.1:p.Pro1081=
|
|
XM_011538731.1:c.3161C=
|
XP_011537033.1:p.Pro1054=
|
|
XM_006719593.3:c.3242C=
|
XP_006719656.1:p.Pro1081=
|
|
XM_011538731.2:c.3161C=
|
XP_011537033.1:p.Pro1054=
|
|
XM_017019961.1:c.3026C=
|
XP_016875450.1:p.Pro1009=
|
|
XM_017019962.2:c.2015C=
|
XP_016875451.1:p.Pro672=
|
|
NM_024312.5:c.3242C=
MANE Select
|
NP_077288.2:p.Pro1081=
|
|