ENST00000485303.6:c.848G>A
MANE Select
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ENSP00000418070.1:p.Gly283Glu
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ENST00000319792.7:c.848G>A
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ENSP00000321514.3:p.Gly283Glu
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ENST00000485303.5:c.848G>A
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ENSP00000418070.1:p.Gly283Glu
|
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ENST00000486596.5:c.549G>A
|
|
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ENST00000493615.5:c.779G>A
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ENSP00000420579.1:p.Gly260Glu
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NM_001243286.1:c.848G>A
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NP_001230215.1:p.Gly283Glu
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NM_001243288.1:c.779G>A
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NP_001230217.1:p.Gly260Glu
|
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NM_015480.2:c.848G>A
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NP_056295.1:p.Gly283Glu
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XM_005247322.3:c.848G>A
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XP_005247379.2:p.Gly283Glu
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XM_011512662.1:c.941G>A
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XP_011510964.1:p.Gly314Glu
|
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XM_011512663.1:c.941G>A
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XP_011510965.1:p.Gly314Glu
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XM_011512664.1:c.779G>A
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XP_011510966.1:p.Gly260Glu
|
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XM_011512665.1:c.941G>A
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XP_011510967.1:p.Gly314Glu
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|
XM_011512666.1:c.941G>A
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XP_011510968.1:p.Gly314Glu
|
|
XM_011512667.1:c.212G>A
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XP_011510969.1:p.Gly71Glu
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XR_924122.1:n.1171G>A
|
|
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XM_017006123.1:c.941G>A
|
XP_016861612.1:p.Gly314Glu
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XM_017006124.1:c.803G>A
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XP_016861613.1:p.Gly268Glu
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XM_017006125.1:c.779G>A
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XP_016861614.1:p.Gly260Glu
|
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XM_017006126.1:c.848G>A
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XP_016861615.1:p.Gly283Glu
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XM_017006127.2:c.212G>A
|
XP_016861616.1:p.Gly71Glu
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XR_002959508.1:n.1129G>A
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|
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XR_924122.2:n.1171G>A
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|
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NM_015480.3:c.848G>A
MANE Select
|
NP_056295.1:p.Gly283Glu
|
|
NM_001243286.2:c.848G>A
|
NP_001230215.1:p.Gly283Glu
|
|
NM_001243288.2:c.779G>A
|
NP_001230217.1:p.Gly260Glu
|
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