ENST00000227266.10:c.1064G>C
MANE Select
|
ENSP00000227266.4:p.Cys355Ser
|
|
ENST00000533897.2:n.5377G>C
|
|
|
ENST00000676612.1:c.*871G>C
|
ENSP00000504440.1:n.*871G>C
|
|
ENST00000677208.1:c.*570G>C
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ENSP00000504347.1:n.*570G>C
|
|
ENST00000677661.1:c.*741G>C
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ENSP00000503323.1:n.*741G>C
|
|
ENST00000677802.1:c.*741G>C
|
ENSP00000504115.1:n.*741G>C
|
|
ENST00000678395.1:c.*570G>C
|
ENSP00000503123.1:n.*570G>C
|
|
ENST00000678464.1:c.1031G>C
|
ENSP00000503046.1:p.Cys344Ser
|
|
ENST00000678506.1:c.1025G>C
|
ENSP00000503580.1:p.Cys342Ser
|
|
ENST00000678520.1:c.*715G>C
|
ENSP00000503361.1:n.*715G>C
|
|
ENST00000678554.1:c.889+1799G>C
|
ENSP00000504541.1:n.889+1799G>C
|
|
ENST00000678915.1:c.932G>C
|
ENSP00000504805.1:p.Cys311Ser
|
|
ENST00000679224.1:c.701G>C
|
ENSP00000504475.1:p.Cys234Ser
|
|
ENST00000227266.9:c.1064G>C
|
ENSP00000227266.4:p.Cys355Ser
|
|
ENST00000533897.1:n.3798G>C
|
|
|
NM_001814.4:c.1064G>C , LRG_50t1:c.1064G>C
|
NP_001805.3:p.Cys355Ser
|
|
NM_001814.5:c.1064G>C
|
NP_001805.3:p.Cys355Ser
|
|
NM_001814.6:c.1064G>C
MANE Select
|
NP_001805.4:p.Cys355Ser
|
|