ENST00000601549.2:n.530T>C
|
|
|
ENST00000648053.1:n.340T>C
|
|
|
ENST00000648319.1:c.908T>C
MANE Select
|
ENSP00000496939.1:p.Met303Thr
|
|
ENST00000262888.7:c.908T>C
|
ENSP00000262888.3:p.Met303Thr
|
|
ENST00000598836.1:c.87T>C
|
|
|
ENST00000599720.5:c.*178T>C
|
ENSP00000472513.1:n.*178T>C
|
|
ENST00000600408.1:c.197T>C
|
ENSP00000472510.1:p.Met66Thr
|
|
ENST00000601549.1:n.217T>C
|
|
|
ENST00000615047.4:c.512T>C
|
ENSP00000485014.1:p.Met171Thr
|
|
NM_002250.2:c.908T>C
|
NP_002241.1:p.Met303Thr
|
|
XM_005258882.2:c.812T>C
|
XP_005258939.1:p.Met271Thr
|
|
XM_005258883.2:c.719T>C
|
XP_005258940.1:p.Met240Thr
|
|
XR_935823.1:n.2154T>C
|
|
|
XR_002958313.1:n.2300T>C
|
|
|
NM_002250.3:c.908T>C
MANE Select
|
NP_002241.1:p.Met303Thr
|
|