ENST00000248633.9:c.2699T>C
MANE Select
|
ENSP00000248633.4:p.Met900Thr
|
|
ENST00000248633.8:c.2699T>C
|
ENSP00000248633.4:p.Met900Thr
|
|
ENST00000428214.5:c.2528T>C
|
ENSP00000394413.1:p.Met843Thr
|
|
ENST00000438045.5:c.1733T>C
|
ENSP00000410438.1:p.Met578Thr
|
|
ENST00000484913.5:n.2738T>C
|
|
|
ENST00000496420.5:n.2591T>C
|
|
|
NM_000466.2:c.2699T>C
|
NP_000457.1:p.Met900Thr
|
|
NM_001282677.1:c.2528T>C
|
NP_001269606.1:p.Met843Thr
|
|
NM_001282678.1:c.2075T>C
|
NP_001269607.1:p.Met692Thr
|
|
XM_005250433.3:c.950T>C
|
XP_005250490.1:p.Met317Thr
|
|
XR_242246.3:n.2795T>C
|
|
|
XM_017012319.2:c.950T>C
|
XP_016867808.1:p.Met317Thr
|
|
XR_001744808.2:n.1726T>C
|
|
|
XR_242246.5:n.2746T>C
|
|
|
NM_000466.3:c.2699T>C
MANE Select
|
NP_000457.1:p.Met900Thr
|
|
NM_001282677.2:c.2528T>C
|
NP_001269606.1:p.Met843Thr
|
|
NM_001282678.2:c.2075T>C
|
NP_001269607.1:p.Met692Thr
|
|