ENST00000295754.10:c.1061T>A
MANE Select
|
ENSP00000295754.5:p.Leu354His
|
|
ENST00000672866.1:n.2657T>A
|
|
|
ENST00000295754.9:c.1061T>A
|
ENSP00000295754.5:p.Leu354His
|
|
ENST00000359013.4:c.1136T>A
|
ENSP00000351905.4:p.Leu379His
|
|
NM_001024847.2:c.1136T>A , LRG_779t1:c.1136T>A
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NP_001020018.1:p.Leu379His
|
|
NM_003242.5:c.1061T>A
|
NP_003233.4:p.Leu354His
|
|
XM_011534043.1:c.1088T>A
|
XP_011532345.1:p.Leu363His
|
|
XM_011534044.1:c.1013T>A
|
XP_011532346.1:p.Leu338His
|
|
XM_011534045.1:c.956T>A
|
XP_011532347.1:p.Leu319His
|
|
XM_011534043.2:c.1088T>A
|
XP_011532345.1:p.Leu363His
|
|
XM_011534045.3:c.956T>A
|
XP_011532347.1:p.Leu319His
|
|
XM_017007106.1:c.956T>A
|
XP_016862595.1:p.Leu319His
|
|
NM_003242.6:c.1061T>A
MANE Select
|
NP_003233.4:p.Leu354His
|
|