ENST00000318158.11:c.558G>C
MANE Select
|
ENSP00000313432.6:p.Gln186His
|
|
ENST00000318158.10:c.558G>C
|
ENSP00000313432.6:p.Gln186His
|
|
ENST00000377824.8:n.595G>C
|
|
|
ENST00000460882.5:n.585G>C
|
|
|
ENST00000480596.5:n.1259G>C
|
|
|
ENST00000482603.1:n.11G>C
|
|
|
ENST00000491488.5:n.263G>C
|
|
|
ENST00000494290.1:c.129G>C
|
ENSP00000432021.1:p.Gln43His
|
|
ENST00000497693.1:n.2091G>C
|
|
|
ENST00000607784.1:c.558G>C
|
ENSP00000475569.1:p.Gln186His
|
|
NM_012203.1:c.558G>C
|
NP_036335.1:p.Gln186His
|
|
XM_005251631.1:c.237G>C
|
XP_005251688.1:p.Gln79His
|
|
XM_011518073.1:c.156G>C
|
XP_011516375.1:p.Gln52His
|
|
XR_929374.1:n.1003G>C
|
|
|
XM_017015320.2:c.558G>C
|
XP_016870809.1:p.Gln186His
|
|
XM_017015321.2:c.558G>C
|
XP_016870810.1:p.Gln186His
|
|
XM_017015323.2:c.156G>C
|
XP_016870812.1:p.Gln52His
|
|
XM_024447716.1:c.831G>C
|
XP_024303484.1:p.Gln277His
|
|
XM_024447717.1:c.831G>C
|
XP_024303485.1:p.Gln277His
|
|
XR_002956828.1:n.846G>C
|
|
|
XR_002956829.1:n.846G>C
|
|
|
XR_002956830.1:n.617G>C
|
|
|
XR_002956831.1:n.292G>C
|
|
|
XR_002956832.1:n.977G>C
|
|
|
NM_012203.2:c.558G>C
MANE Select
|
NP_036335.1:p.Gln186His
|
|