ENST00000686666.1:c.3347G>A
(MED12L)
|
ENSP00000509482.1:p.Arg1116Gln
|
|
ENST00000687756.1:c.3734G>A
(MED12L)
MANE Select
|
ENSP00000508695.1:p.Arg1245Gln
|
|
ENST00000302632.4:c.-180+12056C>T
(P2RY12)
MANE Select
|
ENSP00000307259.4:n.-180+12056C>T
|
|
ENST00000273432.8:c.3209G>A
(MED12L)
|
ENSP00000273432.4:p.Arg1070Gln
|
|
ENST00000302632.3:c.-180+12056C>T
(P2RY12)
|
ENSP00000307259.3:n.-180+12056C>T
|
|
ENST00000474524.5:c.3629G>A
(MED12L)
|
ENSP00000417235.1:p.Arg1210Gln
|
|
NM_022788.4:c.-180+12056C>T , LRG_569t1:c.-180+12056C>T
(P2RY12)
|
NP_073625.1:n.-180+12056C>T
|
|
NM_053002.5:c.3629G>A
(MED12L)
|
NP_443728.3:p.Arg1210Gln
|
|
XM_006713487.2:c.3734G>A
(MED12L)
|
XP_006713550.1:p.Arg1245Gln
|
|
XM_011512386.1:c.3734G>A
(MED12L)
|
XP_011510688.1:p.Arg1245Gln
|
|
XM_011512387.1:c.3731G>A
(MED12L)
|
XP_011510689.1:p.Arg1244Gln
|
|
XM_011512388.1:c.3734G>A
(MED12L)
|
XP_011510690.1:p.Arg1245Gln
|
|
XM_011512389.1:c.3629G>A
(MED12L)
|
XP_011510691.1:p.Arg1210Gln
|
|
XM_011512390.1:c.3629G>A
(MED12L)
|
XP_011510692.1:p.Arg1210Gln
|
|
XM_011512391.1:c.3464G>A
(MED12L)
|
XP_011510693.1:p.Arg1155Gln
|
|
XM_011512392.1:c.3278G>A
(MED12L)
|
XP_011510694.1:p.Arg1093Gln
|
|
XM_011512393.1:c.3734G>A
(MED12L)
|
XP_011510695.1:p.Arg1245Gln
|
|
XM_011512394.1:c.3734G>A
(MED12L)
|
XP_011510696.1:p.Arg1245Gln
|
|
XM_011512395.1:c.3734G>A
(MED12L)
|
XP_011510697.1:p.Arg1245Gln
|
|
XM_011512396.1:c.2159G>A
(MED12L)
|
XP_011510698.1:p.Arg720Gln
|
|
XM_011512397.1:c.1601G>A
(MED12L)
|
XP_011510699.1:p.Arg534Gln
|
|
XM_011512398.1:c.1529G>A
(MED12L)
|
XP_011510700.1:p.Arg510Gln
|
|
XM_011512400.1:c.551G>A
(MED12L)
|
XP_011510702.1:p.Arg184Gln
|
|
XM_006713487.3:c.3734G>A
(MED12L)
|
XP_006713550.1:p.Arg1245Gln
|
|
XM_011512390.2:c.3629G>A
(MED12L)
|
XP_011510692.1:p.Arg1210Gln
|
|
XM_011512394.2:c.3734G>A
(MED12L)
|
XP_011510696.1:p.Arg1245Gln
|
|
XM_017005676.1:c.3734G>A
(MED12L)
|
XP_016861165.1:p.Arg1245Gln
|
|
XM_017005677.1:c.3731G>A
(MED12L)
|
XP_016861166.1:p.Arg1244Gln
|
|
XM_017005678.1:c.3734G>A
(MED12L)
|
XP_016861167.1:p.Arg1245Gln
|
|
XM_017005679.1:c.3464G>A
(MED12L)
|
XP_016861168.1:p.Arg1155Gln
|
|
XM_017005680.1:c.3452G>A
(MED12L)
|
XP_016861169.1:p.Arg1151Gln
|
|
XM_017005681.1:c.1121G>A
(MED12L)
|
XP_016861170.1:p.Arg374Gln
|
|
XR_001740000.1:n.4135G>A
(MED12L)
|
|
|
NM_022788.5:c.-180+12056C>T
(P2RY12)
MANE Select
|
NP_073625.1:n.-180+12056C>T
|
|
NM_001393769.1:c.3734G>A
(MED12L)
MANE Select
|
NP_001380698.1:p.Arg1245Gln
|
|
NM_053002.6:c.3629G>A
(MED12L)
|
NP_443728.3:p.Arg1210Gln
|
|