ENST00000221930.6:c.713G>C
MANE Select
|
ENSP00000221930.4:p.Gly238Ala
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ENST00000600196.2:c.712+140G>C
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ENSP00000504008.1:n.712+140G>C
|
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ENST00000677934.1:c.634+2717G>C
|
ENSP00000504769.1:n.634+2717G>C
|
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ENST00000221930.5:c.713G>C
|
ENSP00000221930.4:p.Gly238Ala
|
|
ENST00000597453.1:n.383G>C
|
|
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ENST00000598758.5:c.1G>C
|
|
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ENST00000600196.1:n.172+140G>C
|
|
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NM_000660.5:c.713G>C
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NP_000651.3:p.Gly238Ala
|
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XM_011527242.1:c.716G>C
|
XP_011525544.1:p.Gly239Ala
|
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NM_000660.6:c.713G>C
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NP_000651.3:p.Gly238Ala
|
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XM_011527242.2:c.716G>C
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XP_011525544.1:p.Gly239Ala
|
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NM_000660.7:c.713G>C
MANE Select
|
NP_000651.3:p.Gly238Ala
|
|