ENST00000699903.1:c.57G>T
|
ENSP00000514679.1:p.Pro19=
|
|
ENST00000699904.1:c.57G>T
|
ENSP00000514680.1:p.Pro19=
|
|
ENST00000699955.1:c.96G>T
|
ENSP00000514715.1:p.Pro32=
|
|
ENST00000561208.6:c.96G>T
MANE Select
|
ENSP00000453793.1:p.Pro32=
|
|
ENST00000314177.12:c.96G>T
|
ENSP00000326296.8:p.Pro32=
|
|
ENST00000338564.9:c.96G>T
|
ENSP00000341400.4:p.Pro32=
|
|
ENST00000340545.9:c.57G>T
|
ENSP00000339549.5:p.Pro19=
|
|
ENST00000397620.6:c.-146G>T
|
ENSP00000380745.2:n.-146G>T
|
|
ENST00000397624.7:c.-146G>T
|
ENSP00000380749.3:n.-146G>T
|
|
ENST00000424352.6:c.96G>T
|
ENSP00000404185.2:p.Pro32=
|
|
ENST00000557796.6:c.57G>T
|
ENSP00000452693.2:p.Pro19=
|
|
ENST00000558313.5:c.-146G>T
|
ENSP00000453782.2:n.-146G>T
|
|
ENST00000559085.5:c.57G>T
|
ENSP00000453390.1:p.Pro19=
|
|
ENST00000559561.5:c.96G>T
|
ENSP00000453497.1:p.Pro32=
|
|
ENST00000560570.5:c.96G>T
|
ENSP00000453481.1:p.Pro32=
|
|
ENST00000561163.5:n.416G>T
|
|
|
ENST00000561208.5:c.96G>T
|
ENSP00000453793.1:p.Pro32=
|
|
NM_001220482.1:c.96G>T
|
NP_001207411.1:p.Pro32=
|
|
NM_002399.3:c.57G>T
|
NP_002390.1:p.Pro19=
|
|
NM_170674.4:c.96G>T
|
NP_733774.1:p.Pro32=
|
|
NM_170675.4:c.96G>T
|
NP_733775.1:p.Pro32=
|
|
NM_170676.4:c.96G>T
|
NP_733776.1:p.Pro32=
|
|
NM_170677.4:c.96G>T
|
NP_733777.1:p.Pro32=
|
|
NM_172315.2:c.57G>T
|
NP_758526.1:p.Pro19=
|
|
NM_172316.2:c.-146G>T
|
NP_758527.1:n.-146G>T
|
|
NR_051953.1:n.770G>T
|
|
|
XM_006720522.2:c.96G>T
|
XP_006720585.1:p.Pro32=
|
|
XM_006720523.1:c.93G>T
|
XP_006720586.1:p.Pro31=
|
|
XM_006720524.1:c.93G>T
|
XP_006720587.1:p.Pro31=
|
|
XM_006720525.1:c.93G>T
|
XP_006720588.1:p.Pro31=
|
|
XM_006720526.2:c.-146G>T
|
XP_006720589.1:n.-146G>T
|
|
XM_006720527.2:c.-201G>T
|
XP_006720590.1:n.-201G>T
|
|
XM_006720528.2:c.-51-2502G>T
|
XP_006720591.1:n.-51-2502G>T
|
|
XM_006720529.2:c.-201G>T
|
XP_006720592.1:n.-201G>T
|
|
XM_006720526.3:c.-146G>T
|
XP_006720589.1:n.-146G>T
|
|
XM_006720527.3:c.-201G>T
|
XP_006720590.1:n.-201G>T
|
|
XM_006720529.3:c.-201G>T
|
XP_006720592.1:n.-201G>T
|
|
XM_017022205.2:c.-146G>T
|
XP_016877694.1:n.-146G>T
|
|
XM_024449925.1:c.57G>T
|
XP_024305693.1:p.Pro19=
|
|
XM_024449926.1:c.57G>T
|
XP_024305694.1:p.Pro19=
|
|
XM_024449927.1:c.57G>T
|
XP_024305695.1:p.Pro19=
|
|
XM_024449928.1:c.-146G>T
|
XP_024305696.1:n.-146G>T
|
|
XM_024449929.1:c.57G>T
|
XP_024305697.1:p.Pro19=
|
|
XR_001751290.2:n.531G>T
|
|
|
XR_002957640.1:n.484G>T
|
|
|
XR_002957641.1:n.484G>T
|
|
|
NM_170675.5:c.96G>T
MANE Select
|
NP_733775.1:p.Pro32=
|
|
NM_001220482.2:c.96G>T
|
NP_001207411.1:p.Pro32=
|
|
NM_170674.5:c.96G>T
|
NP_733774.1:p.Pro32=
|
|
NM_170676.5:c.96G>T
|
NP_733776.1:p.Pro32=
|
|
NM_170677.5:c.96G>T
|
NP_733777.1:p.Pro32=
|
|
NM_172315.3:c.57G>T
|
NP_758526.1:p.Pro19=
|
|
NR_051953.2:n.1179G>T
|
|
|
NM_002399.4:c.57G>T
|
NP_002390.1:p.Pro19=
|
|
NM_172316.3:c.-146G>T
|
NP_758527.1:n.-146G>T
|
|