ENST00000261609.13:c.11807G>C
MANE Select
|
ENSP00000261609.8:p.Trp3936Ser
|
|
ENST00000650509.1:c.3518G>C
|
ENSP00000496936.1:p.Trp1173Ser
|
|
ENST00000261609.11:c.11807G>C
|
ENSP00000261609.7:p.Trp3936Ser
|
|
ENST00000564519.1:n.322G>C
|
|
|
NM_004667.5:c.11807G>C
|
NP_004658.3:p.Trp3936Ser
|
|
XM_005268276.3:c.11693G>C
|
XP_005268333.1:p.Trp3898Ser
|
|
XM_005268277.3:c.11693G>C
|
XP_005268334.1:p.Trp3898Ser
|
|
XM_006720726.2:c.11792G>C
|
XP_006720789.1:p.Trp3931Ser
|
|
XM_006720727.2:c.11549G>C
|
XP_006720790.1:p.Trp3850Ser
|
|
XM_011522131.1:c.11324G>C
|
XP_011520433.1:p.Trp3775Ser
|
|
XM_011522132.1:c.9323G>C
|
XP_011520434.1:p.Trp3108Ser
|
|
XM_011522133.1:c.8552G>C
|
XP_011520435.1:p.Trp2851Ser
|
|
XM_011522134.1:c.5924G>C
|
XP_011520436.1:p.Trp1975Ser
|
|
XM_005268276.5:c.11693G>C
|
XP_005268333.1:p.Trp3898Ser
|
|
XM_006720726.3:c.11792G>C
|
XP_006720789.1:p.Trp3931Ser
|
|
XM_006720727.3:c.11549G>C
|
XP_006720790.1:p.Trp3850Ser
|
|
XM_017022695.1:c.11693G>C
|
XP_016878184.1:p.Trp3898Ser
|
|
XM_017022696.1:c.11693G>C
|
XP_016878185.1:p.Trp3898Ser
|
|
XM_017022697.1:c.4973G>C
|
XP_016878186.1:p.Trp1658Ser
|
|
XM_017022698.1:c.4973G>C
|
XP_016878187.1:p.Trp1658Ser
|
|
NM_004667.6:c.11807G>C
MANE Select
|
NP_004658.3:p.Trp3936Ser
|
|