ENST00000374490.8:c.741G>C
MANE Select
|
ENSP00000363614.3:p.Met247Ile
|
|
ENST00000235958.4:c.311G>C
|
|
|
ENST00000374487.6:c.*782G>C
|
ENSP00000363611.2:n.*782G>C
|
|
ENST00000374490.7:c.741G>C
|
ENSP00000363614.3:p.Met247Ile
|
|
ENST00000436439.6:c.528G>C
|
ENSP00000389281.2:p.Met176Ile
|
|
ENST00000496907.1:n.376G>C
|
|
|
ENST00000509389.5:n.432G>C
|
|
|
NM_000191.2:c.741G>C
|
NP_000182.2:p.Met247Ile
|
|
NM_001166059.1:c.528G>C
|
NP_001159531.1:p.Met176Ile
|
|
NM_000191.3:c.741G>C
MANE Select
|
NP_000182.2:p.Met247Ile
|
|
NM_001166059.2:c.528G>C
|
NP_001159531.1:p.Met176Ile
|
|