ENST00000264670.11:c.744G>C
MANE Select
|
ENSP00000264670.6:p.Arg248Ser
|
|
ENST00000264670.10:c.744G>C
|
ENSP00000264670.6:p.Arg248Ser
|
|
ENST00000504374.5:c.*50G>C
|
ENSP00000421783.1:n.*50G>C
|
|
ENST00000505264.1:n.411G>C
|
|
|
ENST00000505892.5:n.1313G>C
|
|
|
ENST00000506139.5:c.639G>C
|
ENSP00000420957.1:p.Arg213Ser
|
|
NM_001193455.1:c.639G>C
|
NP_001180384.1:p.Arg213Ser
|
|
NM_017755.5:c.744G>C
|
NP_060225.4:p.Arg248Ser
|
|
NR_037947.1:n.1040G>C
|
|
|
NM_017755.6:c.744G>C
MANE Select
|
NP_060225.4:p.Arg248Ser
|
|
NM_001193455.2:c.639G>C
|
NP_001180384.1:p.Arg213Ser
|
|
NR_037947.2:n.724G>C
|
|
|