ENST00000295754.10:c.713A>C
MANE Select
|
ENSP00000295754.5:p.Asn238Thr
|
|
ENST00000672866.1:n.2309A>C
|
|
|
ENST00000295754.9:c.713A>C
|
ENSP00000295754.5:p.Asn238Thr
|
|
ENST00000359013.4:c.788A>C
|
ENSP00000351905.4:p.Asn263Thr
|
|
NM_001024847.2:c.788A>C , LRG_779t1:c.788A>C
|
NP_001020018.1:p.Asn263Thr
|
|
NM_003242.5:c.713A>C
|
NP_003233.4:p.Asn238Thr
|
|
XM_011534043.1:c.740A>C
|
XP_011532345.1:p.Asn247Thr
|
|
XM_011534044.1:c.665A>C
|
XP_011532346.1:p.Asn222Thr
|
|
XM_011534045.1:c.608A>C
|
XP_011532347.1:p.Asn203Thr
|
|
XM_011534043.2:c.740A>C
|
XP_011532345.1:p.Asn247Thr
|
|
XM_011534045.3:c.608A>C
|
XP_011532347.1:p.Asn203Thr
|
|
XM_017007106.1:c.608A>C
|
XP_016862595.1:p.Asn203Thr
|
|
NM_003242.6:c.713A>C
MANE Select
|
NP_003233.4:p.Asn238Thr
|
|