ENST00000685357.1:n.2509-11281A>C
(MED12L)
|
|
|
ENST00000686666.1:c.1864-11281A>C
(MED12L)
|
ENSP00000509482.1:n.1864-11281A>C
|
|
ENST00000687756.1:c.2251-11281A>C
(MED12L)
MANE Select
|
ENSP00000508695.1:n.2251-11281A>C
|
|
ENST00000693531.1:n.2326-11281A>C
(MED12L)
|
|
|
ENST00000302632.4:c.68T>G
(P2RY12)
MANE Select
|
ENSP00000307259.4:p.Ile23Ser
|
|
ENST00000273432.8:c.1726-11281A>C
(MED12L)
|
ENSP00000273432.4:n.1726-11281A>C
|
|
ENST00000302632.3:c.68T>G
(P2RY12)
|
ENSP00000307259.3:p.Ile23Ser
|
|
ENST00000468305.1:n.328-11281A>C
(MED12L)
|
|
|
ENST00000468596.1:n.340T>G
(P2RY12)
|
|
|
ENST00000474524.5:c.2146-11281A>C
(MED12L)
|
ENSP00000417235.1:n.2146-11281A>C
|
|
ENST00000491549.5:n.74-11281A>C
(MED12L)
|
|
|
NM_022788.4:c.68T>G , LRG_569t1:c.68T>G
(P2RY12)
|
NP_073625.1:p.Ile23Ser
|
|
NM_053002.5:c.2146-11281A>C
(MED12L)
|
NP_443728.3:n.2146-11281A>C
|
|
NM_176876.2:c.68T>G
(P2RY12)
|
NP_795345.1:p.Ile23Ser
|
|
XM_006713487.2:c.2251-11281A>C
(MED12L)
|
XP_006713550.1:n.2251-11281A>C
|
|
XM_011512386.1:c.2251-11281A>C
(MED12L)
|
XP_011510688.1:n.2251-11281A>C
|
|
XM_011512387.1:c.2251-11281A>C
(MED12L)
|
XP_011510689.1:n.2251-11281A>C
|
|
XM_011512388.1:c.2251-11281A>C
(MED12L)
|
XP_011510690.1:n.2251-11281A>C
|
|
XM_011512389.1:c.2146-11281A>C
(MED12L)
|
XP_011510691.1:n.2146-11281A>C
|
|
XM_011512390.1:c.2146-11281A>C
(MED12L)
|
XP_011510692.1:n.2146-11281A>C
|
|
XM_011512391.1:c.1981-11281A>C
(MED12L)
|
XP_011510693.1:n.1981-11281A>C
|
|
XM_011512392.1:c.1795-11281A>C
(MED12L)
|
XP_011510694.1:n.1795-11281A>C
|
|
XM_011512393.1:c.2251-11281A>C
(MED12L)
|
XP_011510695.1:n.2251-11281A>C
|
|
XM_011512394.1:c.2251-11281A>C
(MED12L)
|
XP_011510696.1:n.2251-11281A>C
|
|
XM_011512395.1:c.2251-11281A>C
(MED12L)
|
XP_011510697.1:n.2251-11281A>C
|
|
XM_011512396.1:c.676-11281A>C
(MED12L)
|
XP_011510698.1:n.676-11281A>C
|
|
XM_011512398.1:c.46-11281A>C
(MED12L)
|
XP_011510700.1:n.46-11281A>C
|
|
XM_011512399.1:c.2251-11281A>C
(MED12L)
|
XP_011510701.1:n.2251-11281A>C
|
|
XM_006713487.3:c.2251-11281A>C
(MED12L)
|
XP_006713550.1:n.2251-11281A>C
|
|
XM_011512390.2:c.2146-11281A>C
(MED12L)
|
XP_011510692.1:n.2146-11281A>C
|
|
XM_011512394.2:c.2251-11281A>C
(MED12L)
|
XP_011510696.1:n.2251-11281A>C
|
|
XM_011512399.3:c.2251-11281A>C
(MED12L)
|
XP_011510701.1:n.2251-11281A>C
|
|
XM_017005676.1:c.2251-11281A>C
(MED12L)
|
XP_016861165.1:n.2251-11281A>C
|
|
XM_017005677.1:c.2251-11281A>C
(MED12L)
|
XP_016861166.1:n.2251-11281A>C
|
|
XM_017005678.1:c.2251-11281A>C
(MED12L)
|
XP_016861167.1:n.2251-11281A>C
|
|
XM_017005679.1:c.1981-11281A>C
(MED12L)
|
XP_016861168.1:n.1981-11281A>C
|
|
XM_017005680.1:c.1969-11281A>C
(MED12L)
|
XP_016861169.1:n.1969-11281A>C
|
|
XR_001740000.1:n.2652-11281A>C
(MED12L)
|
|
|
NM_022788.5:c.68T>G
(P2RY12)
MANE Select
|
NP_073625.1:p.Ile23Ser
|
|
NM_176876.3:c.68T>G
(P2RY12)
|
NP_795345.1:p.Ile23Ser
|
|
NM_001393769.1:c.2251-11281A>C
(MED12L)
MANE Select
|
NP_001380698.1:n.2251-11281A>C
|
|
NM_053002.6:c.2146-11281A>C
(MED12L)
|
NP_443728.3:n.2146-11281A>C
|
|