ENST00000681320.1:c.7475G>C
MANE Select
|
ENSP00000506558.1:p.Arg2492Pro
|
|
ENST00000328333.12:c.7475G>C
|
ENSP00000332371.8:p.Arg2492Pro
|
|
ENST00000422991.1:c.470G>C
|
ENSP00000391608.1:p.Arg157Pro
|
|
ENST00000459756.5:n.298G>C
|
|
|
ENST00000467985.1:n.321G>C
|
|
|
ENST00000487017.5:n.4114G>C
|
|
|
NM_000094.3:c.7475G>C , LRG_286t1:c.7475G>C
|
NP_000085.1:p.Arg2492Pro
|
|
XM_011533336.1:c.7502G>C
|
XP_011531638.1:p.Arg2501Pro
|
|
XM_011533337.1:c.7475G>C
|
XP_011531639.1:p.Arg2492Pro
|
|
XM_011533338.1:c.7442G>C
|
XP_011531640.1:p.Arg2481Pro
|
|
XM_011533339.1:c.7502G>C
|
XP_011531641.1:p.Arg2501Pro
|
|
XM_011533342.1:c.*30G>C
|
XP_011531644.1:n.*30G>C
|
|
XR_940369.1:n.7538G>C
|
|
|
XR_940370.1:n.7538G>C
|
|
|
XR_940371.1:n.7538G>C
|
|
|
XR_940372.1:n.7512G>C
|
|
|
XM_017005688.1:c.7415G>C
|
XP_016861177.1:p.Arg2472Pro
|
|
XM_017005689.1:c.7475G>C
|
XP_016861178.1:p.Arg2492Pro
|
|
XM_017005692.1:c.*30G>C
|
XP_016861181.1:n.*30G>C
|
|
XR_001740003.1:n.7511G>C
|
|
|
XR_001740004.1:n.7511G>C
|
|
|
XR_001740005.1:n.7511G>C
|
|
|
XR_001740006.1:n.7485G>C
|
|
|
NM_000094.4:c.7475G>C
MANE Select
|
NP_000085.1:p.Arg2492Pro
|
|