ENST00000261609.13:c.11735G=
MANE Select
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ENSP00000261609.8:p.Ser3912=
|
|
ENST00000650509.1:c.3446G=
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ENSP00000496936.1:p.Ser1149=
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|
ENST00000261609.11:c.11735G=
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ENSP00000261609.7:p.Ser3912=
|
|
ENST00000564519.1:n.250G=
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|
|
NM_004667.5:c.11735G=
|
NP_004658.3:p.Ser3912=
|
|
XM_005268276.3:c.11621G=
|
XP_005268333.1:p.Ser3874=
|
|
XM_005268277.3:c.11621G=
|
XP_005268334.1:p.Ser3874=
|
|
XM_006720726.2:c.11720G=
|
XP_006720789.1:p.Ser3907=
|
|
XM_006720727.2:c.11477G=
|
XP_006720790.1:p.Ser3826=
|
|
XM_011522131.1:c.11252G=
|
XP_011520433.1:p.Ser3751=
|
|
XM_011522132.1:c.9251G=
|
XP_011520434.1:p.Ser3084=
|
|
XM_011522133.1:c.8480G=
|
XP_011520435.1:p.Ser2827=
|
|
XM_011522134.1:c.5852G=
|
XP_011520436.1:p.Ser1951=
|
|
XM_005268276.5:c.11621G=
|
XP_005268333.1:p.Ser3874=
|
|
XM_006720726.3:c.11720G=
|
XP_006720789.1:p.Ser3907=
|
|
XM_006720727.3:c.11477G=
|
XP_006720790.1:p.Ser3826=
|
|
XM_017022695.1:c.11621G=
|
XP_016878184.1:p.Ser3874=
|
|
XM_017022696.1:c.11621G=
|
XP_016878185.1:p.Ser3874=
|
|
XM_017022697.1:c.4901G=
|
XP_016878186.1:p.Ser1634=
|
|
XM_017022698.1:c.4901G=
|
XP_016878187.1:p.Ser1634=
|
|
NM_004667.6:c.11735G=
MANE Select
|
NP_004658.3:p.Ser3912=
|
|