ENST00000340124.9:c.1212+3G>A
MANE Select
|
ENSP00000345282.4:n.1212+3G>A
|
|
ENST00000340124.8:c.1212+3G>A
|
ENSP00000345282.4:n.1212+3G>A
|
|
ENST00000440783.2:c.912+3G>A
|
ENSP00000413804.2:n.912+3G>A
|
|
ENST00000562801.5:n.1722+3G>A
|
|
|
NM_001142466.1:c.912+3G>A
|
NP_001135938.1:n.912+3G>A
|
|
NM_001142466.2:c.912+3G>A
|
NP_001135938.1:n.912+3G>A
|
|
NM_133443.2:c.1212+3G>A
|
NP_597700.1:n.1212+3G>A
|
|
NM_133443.3:c.1212+3G>A
|
NP_597700.1:n.1212+3G>A
|
|
XM_017023790.1:c.780+3G>A
|
XP_016879279.1:n.780+3G>A
|
|
NM_133443.4:c.1212+3G>A
MANE Select
|
NP_597700.1:n.1212+3G>A
|
|
NM_001142466.3:c.912+3G>A
|
NP_001135938.1:n.912+3G>A
|
|