ENST00000221930.6:c.818G>C
MANE Select
|
ENSP00000221930.4:p.Ser273Thr
|
|
ENST00000600196.2:c.712+245G>C
|
ENSP00000504008.1:n.712+245G>C
|
|
ENST00000677934.1:c.634+2822G>C
|
ENSP00000504769.1:n.634+2822G>C
|
|
ENST00000221930.5:c.818G>C
|
ENSP00000221930.4:p.Ser273Thr
|
|
ENST00000598758.5:c.106G>C
|
|
|
ENST00000600196.1:n.172+245G>C
|
|
|
NM_000660.5:c.818G>C
|
NP_000651.3:p.Ser273Thr
|
|
XM_011527242.1:c.821G>C
|
XP_011525544.1:p.Ser274Thr
|
|
NM_000660.6:c.818G>C
|
NP_000651.3:p.Ser273Thr
|
|
XM_011527242.2:c.821G>C
|
XP_011525544.1:p.Ser274Thr
|
|
NM_000660.7:c.818G>C
MANE Select
|
NP_000651.3:p.Ser273Thr
|
|