ENST00000295754.10:c.1022T>C
MANE Select
|
ENSP00000295754.5:p.Val341Ala
|
|
ENST00000672866.1:n.2618T>C
|
|
|
ENST00000295754.9:c.1022T>C
|
ENSP00000295754.5:p.Val341Ala
|
|
ENST00000359013.4:c.1097T>C
|
ENSP00000351905.4:p.Val366Ala
|
|
NM_001024847.2:c.1097T>C , LRG_779t1:c.1097T>C
|
NP_001020018.1:p.Val366Ala
|
|
NM_003242.5:c.1022T>C
|
NP_003233.4:p.Val341Ala
|
|
XM_011534043.1:c.1049T>C
|
XP_011532345.1:p.Val350Ala
|
|
XM_011534044.1:c.974T>C
|
XP_011532346.1:p.Val325Ala
|
|
XM_011534045.1:c.917T>C
|
XP_011532347.1:p.Val306Ala
|
|
XM_011534043.2:c.1049T>C
|
XP_011532345.1:p.Val350Ala
|
|
XM_011534045.3:c.917T>C
|
XP_011532347.1:p.Val306Ala
|
|
XM_017007106.1:c.917T>C
|
XP_016862595.1:p.Val306Ala
|
|
NM_003242.6:c.1022T>C
MANE Select
|
NP_003233.4:p.Val341Ala
|
|