ENST00000318158.11:c.148G=
MANE Select
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ENSP00000313432.6:p.Ala50=
|
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ENST00000318158.10:c.148G=
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ENSP00000313432.6:p.Ala50=
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ENST00000377824.8:n.185G=
|
|
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ENST00000460882.5:n.175G=
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|
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ENST00000487399.5:n.157G=
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ENST00000491488.5:n.109+2076G=
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|
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ENST00000493368.5:n.205G=
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|
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ENST00000607784.1:c.148G=
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ENSP00000475569.1:p.Ala50=
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NM_012203.1:c.148G=
|
NP_036335.1:p.Ala50=
|
|
XM_005251631.1:c.83+2076G=
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XP_005251688.1:n.83+2076G=
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XM_011518073.1:c.-615G=
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XP_011516375.1:n.-615G=
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XR_929374.1:n.233G=
|
|
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XM_017015320.2:c.148G=
|
XP_016870809.1:p.Ala50=
|
|
XM_017015321.2:c.148G=
|
XP_016870810.1:p.Ala50=
|
|
XM_017015323.2:c.-615G=
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XP_016870812.1:n.-615G=
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|
XM_024447716.1:c.421G=
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XP_024303484.1:p.Ala141=
|
|
XM_024447717.1:c.421G=
|
XP_024303485.1:p.Ala141=
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XR_002956828.1:n.436G=
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|
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XR_002956829.1:n.436G=
|
|
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XR_002956830.1:n.207G=
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XR_002956831.1:n.138+2076G=
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|
|
XR_002956832.1:n.207G=
|
|
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NM_012203.2:c.148G=
MANE Select
|
NP_036335.1:p.Ala50=
|
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