ENST00000318158.11:c.944C>T
MANE Select
|
ENSP00000313432.6:p.Ala315Val
|
|
ENST00000318158.10:c.944C>T
|
ENSP00000313432.6:p.Ala315Val
|
|
ENST00000460882.5:n.971C>T
|
|
|
ENST00000480596.5:n.1645C>T
|
|
|
ENST00000494290.1:c.*52-142C>T
|
ENSP00000432021.1:n.*52-142C>T
|
|
ENST00000497693.1:n.4512C>T
|
|
|
NM_012203.1:c.944C>T
|
NP_036335.1:p.Ala315Val
|
|
XM_005251631.1:c.623C>T
|
XP_005251688.1:p.Ala208Val
|
|
XM_011518073.1:c.542C>T
|
XP_011516375.1:p.Ala181Val
|
|
XM_017015320.2:c.946-672C>T
|
XP_016870809.1:n.946-672C>T
|
|
XM_017015321.2:c.866-672C>T
|
XP_016870810.1:n.866-672C>T
|
|
XM_017015323.2:c.544-672C>T
|
XP_016870812.1:n.544-672C>T
|
|
XM_024447716.1:c.1219-672C>T
|
XP_024303484.1:n.1219-672C>T
|
|
XM_024447717.1:c.1139-672C>T
|
XP_024303485.1:n.1139-672C>T
|
|
XR_002956828.1:n.1234-672C>T
|
|
|
XR_002956829.1:n.1154-672C>T
|
|
|
XR_002956830.1:n.2364C>T
|
|
|
XR_002956831.1:n.2039C>T
|
|
|
XR_002956832.1:n.1363C>T
|
|
|
NM_012203.2:c.944C>T
MANE Select
|
NP_036335.1:p.Ala315Val
|
|