|
ENST00000356839.10:c.266C>A
MANE Select
|
ENSP00000349297.5:p.Pro89Gln
|
|
|
ENST00000322910.9:c.*221C>A
|
ENSP00000325395.5:n.*221C>A
|
|
|
ENST00000350303.9:c.200C>A
|
ENSP00000344152.5:p.Pro67Gln
|
|
|
ENST00000356839.9:c.266C>A
|
ENSP00000349297.5:p.Pro89Gln
|
|
|
ENST00000543245.6:c.335C>A
|
ENSP00000438689.2:p.Pro112Gln
|
|
|
ENST00000577191.5:n.343C>A
|
|
|
|
ENST00000577433.5:n.474C>A
|
|
|
|
ENST00000577857.5:n.229-101C>A
|
|
|
|
ENST00000578269.5:n.713C>A
|
|
|
|
ENST00000578421.1:n.474C>A
|
|
|
|
ENST00000579286.5:n.447C>A
|
|
|
|
ENST00000579886.2:c.201+139C>A
|
ENSP00000463246.1:n.201+139C>A
|
|
|
ENST00000580263.5:n.430C>A
|
|
|
|
ENST00000581562.5:n.313C>A
|
|
|
|
ENST00000582056.5:n.356C>A
|
|
|
|
ENST00000582166.1:n.154C>A
|
|
|
|
ENST00000582356.5:n.465C>A
|
|
|
|
ENST00000583312.5:c.266C>A
|
ENSP00000467920.1:p.Pro89Gln
|
|
|
ENST00000584103.5:c.266C>A
|
ENSP00000465353.1:p.Pro89Gln
|
|
|
NM_000018.3:c.266C>A
|
NP_000009.1:p.Pro89Gln
|
|
|
NM_001033859.2:c.200C>A
|
NP_001029031.1:p.Pro67Gln
|
|
|
NM_001270447.1:c.335C>A
|
NP_001257376.1:p.Pro112Gln
|
|
|
NM_001270448.1:c.38C>A
|
NP_001257377.1:p.Pro13Gln
|
|
|
XM_006721516.2:c.266C>A
|
XP_006721579.2:p.Pro89Gln
|
|
|
XM_011523829.1:c.266C>A
|
XP_011522131.1:p.Pro89Gln
|
|
|
XM_011523830.1:c.266C>A
|
XP_011522132.1:p.Pro89Gln
|
|
|
XR_934021.1:n.373C>A
|
|
|
|
XR_934022.1:n.373C>A
|
|
|
|
XR_934023.1:n.373C>A
|
|
|
|
XM_006721516.3:c.266C>A
|
XP_006721579.2:p.Pro89Gln
|
|
|
XM_011523829.2:c.266C>A
|
XP_011522131.1:p.Pro89Gln
|
|
|
XM_011523830.2:c.266C>A
|
XP_011522132.1:p.Pro89Gln
|
|
|
XM_024450741.1:c.266C>A
|
XP_024306509.1:p.Pro89Gln
|
|
|
XR_934021.2:n.325C>A
|
|
|
|
XR_934022.2:n.325C>A
|
|
|
|
XR_934023.2:n.325C>A
|
|
|
|
NM_000018.4:c.266C>A
MANE Select
|
NP_000009.1:p.Pro89Gln
|
|
|
NM_001033859.3:c.200C>A
|
NP_001029031.1:p.Pro67Gln
|
|
|
NM_001270447.2:c.335C>A
|
NP_001257376.1:p.Pro112Gln
|
|
|
NM_001270448.2:c.38C>A
|
NP_001257377.1:p.Pro13Gln
|
|
