ENST00000260408.8:c.425G>T
MANE Select
|
ENSP00000260408.3:p.Arg142Ile
|
|
ENST00000260408.7:c.425G>T
|
ENSP00000260408.3:p.Arg142Ile
|
|
ENST00000396136.6:c.100G>T
|
|
|
ENST00000402627.5:c.56-38353G>T
|
ENSP00000386056.1:n.56-38353G>T
|
|
ENST00000439637.5:c.325+3013G>T
|
ENSP00000391930.1:n.325+3013G>T
|
|
ENST00000497846.5:n.542G>T
|
|
|
ENST00000558004.1:c.332-13986G>T
|
ENSP00000452704.1:n.332-13986G>T
|
|
ENST00000558733.5:n.661G>T
|
|
|
ENST00000559053.1:c.56-38353G>T
|
ENSP00000453952.1:n.56-38353G>T
|
|
ENST00000560608.5:n.563G>T
|
|
|
ENST00000561288.1:c.55+70297G>T
|
ENSP00000452639.1:n.55+70297G>T
|
|
NM_001110.3:c.425G>T
|
NP_001101.1:p.Arg142Ile
|
|
XM_005254117.2:c.425G>T
|
XP_005254174.1:p.Arg142Ile
|
|
NM_001320570.1:c.425G>T
|
NP_001307499.1:p.Arg142Ile
|
|
XM_024449818.1:c.203G>T
|
XP_024305586.1:p.Arg68Ile
|
|
NM_001110.4:c.425G>T
MANE Select
|
NP_001101.1:p.Arg142Ile
|
|
NM_001320570.2:c.425G>T
|
NP_001307499.1:p.Arg142Ile
|
|