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NM_000018.4:c.553G>A
MANE Select
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NP_000009.1:p.Gly185Ser
|
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ENST00000356839.10:c.553G>A
MANE Select
|
ENSP00000349297.5:p.Gly185Ser
|
|
NM_000018.3:c.553G>A
|
NP_000009.1:p.Gly185Ser
|
|
NM_001033859.2:c.487G>A
|
NP_001029031.1:p.Gly163Ser
|
|
NM_001033859.3:c.487G>A
|
NP_001029031.1:p.Gly163Ser
|
|
NM_001270447.1:c.622G>A
|
NP_001257376.1:p.Gly208Ser
|
|
NM_001270447.2:c.622G>A
|
NP_001257376.1:p.Gly208Ser
|
|
NM_001270448.1:c.325G>A
|
NP_001257377.1:p.Gly109Ser
|
|
NM_001270448.2:c.325G>A
|
NP_001257377.1:p.Gly109Ser
|
|
ENST00000322910.9:c.*508G>A
|
ENSP00000325395.5:n.*508G>A
|
|
ENST00000350303.9:c.487G>A
|
ENSP00000344152.5:p.Gly163Ser
|
|
ENST00000356839.9:c.553G>A
|
ENSP00000349297.5:p.Gly185Ser
|
|
ENST00000543245.6:c.622G>A
|
ENSP00000438689.2:p.Gly208Ser
|
|
ENST00000577191.5:n.630G>A
|
|
|
ENST00000577433.5:n.761G>A
|
|
|
ENST00000577857.5:n.369G>A
|
|
|
ENST00000579286.5:n.734G>A
|
|
|
ENST00000579886.2:c.391G>A
|
ENSP00000463246.1:p.Gly131Ser
|
|
ENST00000580365.1:n.284G>A
|
|
|
ENST00000581378.5:c.271G>A
|
|
|
ENST00000581562.5:n.525-339G>A
|
|
|
ENST00000582166.1:n.534G>A
|
|
|
ENST00000583312.5:c.553G>A
|
ENSP00000467920.1:p.Gly185Ser
|
|
ENST00000583760.1:n.335G>A
|
|
|
XM_006721516.2:c.553G>A
|
XP_006721579.2:p.Gly185Ser
|
|
XM_006721516.3:c.553G>A
|
XP_006721579.2:p.Gly185Ser
|
|
XM_011523829.1:c.553G>A
|
XP_011522131.1:p.Gly185Ser
|
|
XM_011523829.2:c.553G>A
|
XP_011522131.1:p.Gly185Ser
|
|
XM_011523830.1:c.553G>A
|
XP_011522132.1:p.Gly185Ser
|
|
XM_011523830.2:c.553G>A
|
XP_011522132.1:p.Gly185Ser
|
|
XM_024450741.1:c.553G>A
|
XP_024306509.1:p.Gly185Ser
|
|
XR_934021.1:n.660G>A
|
|
|
XR_934021.2:n.612G>A
|
|
|
XR_934022.1:n.660G>A
|
|
|
XR_934022.2:n.612G>A
|
|
|
XR_934023.1:n.660G>A
|
|
|
XR_934023.2:n.612G>A
|
|
