ENST00000224721.12:c.5590A>G
MANE Select
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ENSP00000224721.9:p.Ser1864Gly
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ENST00000224721.10:c.5605A>G
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ENSP00000224721.8:p.Ser1869Gly
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ENST00000622827.4:c.5590A>G
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ENSP00000483211.1:p.Ser1864Gly
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NM_022124.5:c.5590A>G
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NP_071407.4:p.Ser1864Gly
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XM_006717940.2:c.5785A>G
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XP_006718003.1:p.Ser1929Gly
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XM_006717942.2:c.5719A>G
|
XP_006718005.1:p.Ser1907Gly
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XM_011540039.1:c.5782A>G
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XP_011538341.1:p.Ser1928Gly
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XM_011540040.1:c.5779A>G
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XP_011538342.1:p.Ser1927Gly
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XM_011540041.1:c.5725A>G
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XP_011538343.1:p.Ser1909Gly
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XM_011540042.1:c.5785A>G
|
XP_011538344.1:p.Ser1929Gly
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|
XM_011540043.1:c.5785A>G
|
XP_011538345.1:p.Ser1929Gly
|
|
XM_011540044.1:c.5650A>G
|
XP_011538346.1:p.Ser1884Gly
|
|
XM_011540045.1:c.5785A>G
|
XP_011538347.1:p.Ser1929Gly
|
|
XM_011540046.1:c.5245A>G
|
XP_011538348.1:p.Ser1749Gly
|
|
XM_011540047.1:c.4603A>G
|
XP_011538349.1:p.Ser1535Gly
|
|
XM_011540048.1:c.5785A>G
|
XP_011538350.1:p.Ser1929Gly
|
|
XM_011540049.1:c.5785A>G
|
XP_011538351.1:p.Ser1929Gly
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|
XM_011540050.1:c.5785A>G
|
XP_011538352.1:p.Ser1929Gly
|
|
XM_011540051.1:c.5785A>G
|
XP_011538353.1:p.Ser1929Gly
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|
XM_011540052.1:c.2113A>G
|
XP_011538354.1:p.Ser705Gly
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|
XM_011540053.1:c.5785A>G
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XP_011538355.1:p.Ser1929Gly
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XR_945796.1:n.6028A>G
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|
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NM_022124.6:c.5590A>G
MANE Select
|
NP_071407.4:p.Ser1864Gly
|
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