ENST00000324001.8:c.2417T>C
MANE Select
|
ENSP00000326018.6:p.Met806Thr
|
|
ENST00000673881.1:c.2000T>C
|
ENSP00000501070.1:p.Met667Thr
|
|
ENST00000674005.2:c.2702T>C
|
ENSP00000501261.1:p.Met901Thr
|
|
ENST00000674773.1:c.2000T>C
|
ENSP00000502579.1:p.Met667Thr
|
|
ENST00000675517.1:c.2292T>C
|
|
|
ENST00000676076.1:c.2278T>C
|
|
|
ENST00000676260.1:c.2379T>C
|
|
|
ENST00000676316.1:c.2304T>C
|
|
|
ENST00000291825.11:c.*2622T>C
|
ENSP00000291825.6:n.*2622T>C
|
|
ENST00000324001.7:c.2417T>C
|
ENSP00000326018.6:p.Met806Thr
|
|
NM_020956.2:c.*2622T>C , LRG_265t1:c.*2622T>C
|
NP_066007.1:n.*2622T>C
|
|
NM_181882.2:c.2417T>C , LRG_265t2:c.2417T>C
|
NP_870998.2:p.Met806Thr
|
|
XM_011527171.1:c.2417T>C
|
XP_011525473.1:p.Met806Thr
|
|
XM_011527171.2:c.2417T>C
|
XP_011525473.1:p.Met806Thr
|
|
XM_017027046.1:c.2315T>C
|
XP_016882535.1:p.Met772Thr
|
|
XM_017027047.1:c.2315T>C
|
XP_016882536.1:p.Met772Thr
|
|
NM_181882.3:c.2417T>C
MANE Select
|
NP_870998.2:p.Met806Thr
|
|