ENST00000594866.3:c.1162C>G
MANE Select
|
ENSP00000469738.2:p.Pro388Ala
|
|
ENST00000614245.2:c.436C>G
|
ENSP00000480219.2:p.Pro146Ala
|
|
ENST00000396720.7:c.1162C>G
|
ENSP00000379946.2:p.Pro388Ala
|
|
ENST00000614245.1:c.1006C>G
|
ENSP00000480219.1:p.Pro336Ala
|
|
NM_015711.3:c.1162C>G
|
NP_056526.3:p.Pro388Ala
|
|
XM_005258833.3:c.1162C>G
|
XP_005258890.1:p.Pro388Ala
|
|
XM_006723180.2:c.1162C>G
|
XP_006723243.1:p.Pro388Ala
|
|
XM_011526882.1:c.1024C>G
|
XP_011525184.1:p.Pro342Ala
|
|
XM_011526883.1:c.1162C>G
|
XP_011525185.1:p.Pro388Ala
|
|
XM_005258833.4:c.1162C>G
|
XP_005258890.1:p.Pro388Ala
|
|
XM_006723180.3:c.1162C>G
|
XP_006723243.1:p.Pro388Ala
|
|
XM_011526882.2:c.1024C>G
|
XP_011525184.1:p.Pro342Ala
|
|
XM_011526883.2:c.1162C>G
|
XP_011525185.1:p.Pro388Ala
|
|
NM_001394372.1:c.1162C>G
MANE Select
|
NP_001381301.1:p.Pro388Ala
|
|