ENST00000318158.11:c.889G>C
MANE Select
|
ENSP00000313432.6:p.Ala297Pro
|
|
ENST00000318158.10:c.889G>C
|
ENSP00000313432.6:p.Ala297Pro
|
|
ENST00000460882.5:n.916G>C
|
|
|
ENST00000480596.5:n.1590G>C
|
|
|
ENST00000491488.5:n.594G>C
|
|
|
ENST00000494290.1:c.*52-197G>C
|
ENSP00000432021.1:n.*52-197G>C
|
|
ENST00000497693.1:n.4457G>C
|
|
|
NM_012203.1:c.889G>C
|
NP_036335.1:p.Ala297Pro
|
|
XM_005251631.1:c.568G>C
|
XP_005251688.1:p.Ala190Pro
|
|
XM_011518073.1:c.487G>C
|
XP_011516375.1:p.Ala163Pro
|
|
XM_017015320.2:c.946-727G>C
|
XP_016870809.1:n.946-727G>C
|
|
XM_017015321.2:c.866-727G>C
|
XP_016870810.1:n.866-727G>C
|
|
XM_017015323.2:c.544-727G>C
|
XP_016870812.1:n.544-727G>C
|
|
XM_024447716.1:c.1219-727G>C
|
XP_024303484.1:n.1219-727G>C
|
|
XM_024447717.1:c.1139-727G>C
|
XP_024303485.1:n.1139-727G>C
|
|
XR_002956828.1:n.1234-727G>C
|
|
|
XR_002956829.1:n.1154-727G>C
|
|
|
XR_002956830.1:n.2309G>C
|
|
|
XR_002956831.1:n.1984G>C
|
|
|
XR_002956832.1:n.1308G>C
|
|
|
NM_012203.2:c.889G>C
MANE Select
|
NP_036335.1:p.Ala297Pro
|
|