ENST00000650516.2:c.1781G>C
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ENSP00000498052.2:p.Gly594Ala
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ENST00000343257.7:c.1781G>C
MANE Select
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ENSP00000339867.2:p.Gly594Ala
|
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ENST00000432192.6:c.1605G>C
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ENST00000343257.6:c.1781G>C
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ENSP00000339867.2:p.Gly594Ala
|
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NM_000083.2:c.1781G>C
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NP_000074.2:p.Gly594Ala
|
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NR_046453.1:n.1721G>C
|
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XM_011515781.1:c.1805G>C
|
XP_011514083.1:p.Gly602Ala
|
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XM_011515782.1:c.527G>C
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XP_011514084.1:p.Gly176Ala
|
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XM_011515782.2:c.527G>C
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XP_011514084.1:p.Gly176Ala
|
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XM_017011739.1:c.1355G>C
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XP_016867228.1:p.Gly452Ala
|
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XM_017011740.1:c.1331G>C
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XP_016867229.1:p.Gly444Ala
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NM_000083.3:c.1781G>C
MANE Select
|
NP_000074.3:p.Gly594Ala
|
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NR_046453.2:n.1736G>C
|
|
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