ENST00000265631.10:c.1780G>C
MANE Select
|
ENSP00000265631.6:p.Gly594Arg
|
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ENST00000265631.9:c.1780G>C
|
ENSP00000265631.5:p.Gly594Arg
|
|
ENST00000416240.6:c.1783G>C
|
ENSP00000400101.2:p.Gly595Arg
|
|
ENST00000494085.1:n.283G>C
|
|
|
NM_001160210.1:c.1783G>C
|
NP_001153682.1:p.Gly595Arg
|
|
NM_014251.2:c.1780G>C
|
NP_055066.1:p.Gly594Arg
|
|
NR_027662.1:n.1855G>C
|
|
|
XM_006715831.2:c.1813G>C
|
XP_006715894.1:p.Gly605Arg
|
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XM_011515728.1:c.928G>C
|
XP_011514030.1:p.Gly310Arg
|
|
XM_006715831.4:c.1813G>C
|
XP_006715894.1:p.Gly605Arg
|
|
XM_017011663.1:c.1771G>C
|
XP_016867152.1:p.Gly591Arg
|
|
XM_017011664.2:c.928G>C
|
XP_016867153.1:p.Gly310Arg
|
|
XM_017011665.1:c.928G>C
|
XP_016867154.1:p.Gly310Arg
|
|
XR_001744525.2:n.2026G>C
|
|
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XR_002956405.1:n.2584G>C
|
|
|
NM_014251.3:c.1780G>C
MANE Select
|
NP_055066.1:p.Gly594Arg
|
|
NR_027662.2:n.1806G>C
|
|
|
NM_001160210.2:c.1783G>C
|
NP_001153682.1:p.Gly595Arg
|
|