ENST00000683572.1:n.790G>A
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ENST00000341947.7:c.4984G>A
MANE Select
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ENSP00000339915.2:p.Gly1662Ser
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ENST00000341947.6:c.4984G>A
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ENSP00000339915.2:p.Gly1662Ser
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ENST00000361917.5:c.4663G>A
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ENSP00000355123.1:p.Gly1555Ser
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ENST00000374708.8:c.4726G>A
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ENSP00000363840.4:p.Gly1576Ser
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ENST00000477772.1:n.774G>A
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NM_080679.2:c.4663G>A
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NP_542410.2:p.Gly1555Ser
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NM_080680.2:c.4984G>A
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NP_542411.2:p.Gly1662Ser
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NM_080681.2:c.4726G>A
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NP_542412.2:p.Gly1576Ser
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XM_011514298.1:c.4138G>A
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XP_011512600.1:p.Gly1380Ser
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XM_011514299.1:c.4270G>A
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XP_011512601.1:p.Gly1424Ser
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XM_011514300.1:c.4090G>A
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XP_011512602.1:p.Gly1364Ser
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XM_011514301.1:c.4027G>A
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XP_011512603.1:p.Gly1343Ser
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XM_011514302.1:c.3871G>A
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XP_011512604.1:p.Gly1291Ser
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XM_011514299.2:c.4270G>A
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XP_011512601.1:p.Gly1424Ser
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XM_011514300.2:c.4090G>A
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XP_011512602.1:p.Gly1364Ser
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XM_011514302.2:c.3871G>A
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XP_011512604.1:p.Gly1291Ser
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XM_017010250.1:c.4984G>A
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XP_016865739.1:p.Gly1662Ser
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|
XM_017010251.2:c.3802G>A
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XP_016865740.1:p.Gly1268Ser
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NM_080680.3:c.4984G>A
MANE Select
|
NP_542411.2:p.Gly1662Ser
|
|
NM_080681.3:c.4726G>A
|
NP_542412.2:p.Gly1576Ser
|
|
NM_080679.3:c.4663G>A
|
NP_542410.2:p.Gly1555Ser
|
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