ENST00000356839.10:c.272C>A
MANE Select
|
ENSP00000349297.5:p.Pro91Gln
|
|
ENST00000322910.9:c.*227C>A
|
ENSP00000325395.5:n.*227C>A
|
|
ENST00000350303.9:c.206C>A
|
ENSP00000344152.5:p.Pro69Gln
|
|
ENST00000356839.9:c.272C>A
|
ENSP00000349297.5:p.Pro91Gln
|
|
ENST00000543245.6:c.341C>A
|
ENSP00000438689.2:p.Pro114Gln
|
|
ENST00000577191.5:n.349C>A
|
|
|
ENST00000577433.5:n.480C>A
|
|
|
ENST00000577857.5:n.229-95C>A
|
|
|
ENST00000578269.5:n.719C>A
|
|
|
ENST00000578421.1:n.480C>A
|
|
|
ENST00000579286.5:n.453C>A
|
|
|
ENST00000579886.2:c.201+145C>A
|
ENSP00000463246.1:n.201+145C>A
|
|
ENST00000580263.5:n.436C>A
|
|
|
ENST00000581562.5:n.319C>A
|
|
|
ENST00000582056.5:n.362C>A
|
|
|
ENST00000582166.1:n.160C>A
|
|
|
ENST00000582356.5:n.471C>A
|
|
|
ENST00000583312.5:c.272C>A
|
ENSP00000467920.1:p.Pro91Gln
|
|
ENST00000584103.5:c.272C>A
|
ENSP00000465353.1:p.Pro91Gln
|
|
NM_000018.3:c.272C>A
|
NP_000009.1:p.Pro91Gln
|
|
NM_001033859.2:c.206C>A
|
NP_001029031.1:p.Pro69Gln
|
|
NM_001270447.1:c.341C>A
|
NP_001257376.1:p.Pro114Gln
|
|
NM_001270448.1:c.44C>A
|
NP_001257377.1:p.Pro15Gln
|
|
XM_006721516.2:c.272C>A
|
XP_006721579.2:p.Pro91Gln
|
|
XM_011523829.1:c.272C>A
|
XP_011522131.1:p.Pro91Gln
|
|
XM_011523830.1:c.272C>A
|
XP_011522132.1:p.Pro91Gln
|
|
XR_934021.1:n.379C>A
|
|
|
XR_934022.1:n.379C>A
|
|
|
XR_934023.1:n.379C>A
|
|
|
XM_006721516.3:c.272C>A
|
XP_006721579.2:p.Pro91Gln
|
|
XM_011523829.2:c.272C>A
|
XP_011522131.1:p.Pro91Gln
|
|
XM_011523830.2:c.272C>A
|
XP_011522132.1:p.Pro91Gln
|
|
XM_024450741.1:c.272C>A
|
XP_024306509.1:p.Pro91Gln
|
|
XR_934021.2:n.331C>A
|
|
|
XR_934022.2:n.331C>A
|
|
|
XR_934023.2:n.331C>A
|
|
|
NM_000018.4:c.272C>A
MANE Select
|
NP_000009.1:p.Pro91Gln
|
|
NM_001033859.3:c.206C>A
|
NP_001029031.1:p.Pro69Gln
|
|
NM_001270447.2:c.341C>A
|
NP_001257376.1:p.Pro114Gln
|
|
NM_001270448.2:c.44C>A
|
NP_001257377.1:p.Pro15Gln
|
|